FDA 510(k), K121976, AESCULAP HISTOACRYL FLEXIBLE TOPICAL SKIN ADHESIVE

FDA 510(k), K121976, AESCULAP HISTOACRYL FLEXIBLE TOPICAL SKIN ADHESIVE

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510(K) Number: K121976
Device Name: AESCULAP HISTOACRYL FLEXIBLE TOPICAL SKIN ADHESIVE
Manufacturer: KATHY A RACOSKY
Device Classification Name: Tissue Adhesive For The Topical Approximation Of Skin
Regulation Number: MPN
Classification Product Code: KXA
Date Received: 07/05/2012
Decision Date: 05/17/2013
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

Total pages: 707
Fully redacted pages: 575
Content pages: 132

PLEASE NOTE: Most 510(k)s obtained through FOIA are heavily redacted, often omitting sections related to testing, software, manufacturing, and other technical data. Please be sure to review the total pages, redacted pages, and content pages listed in the description to get a sense of how much of the document is redacted. As the FDA FOIA office explains: “We HEAVILY REDACT the majority of the following portions of 510(k) filings: testing data, technical data, lab reports, manufacturing information, vendor information, substantive discussions regarding deficiencies or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.” If you’d like more details about a specific document before purchasing, please contact us at info@foiadocs.com.

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