FDA 510(k), K951123, CAVICIDE SURFACE DISINFECTANT/DECONTAMINANT CLEANER

FDA 510(k), K951123, CAVICIDE SURFACE DISINFECTANT/DECONTAMINANT CLEANER

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510(K) Number: K951123
Device Name: CAVICIDE SURFACE DISINFECTANT/DECONTAMINANT CLEANER
Manufacturer:
Device Classification Name: Disinfectant, Medical Devices
Regulation Number: 880.6890
Classification Product Code: LRJ
Date Received: 02/24/1995
Decision Date: 04/25/1995
Regulation Medical Specialty: General Hospital

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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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