FDA 510(k) K864323, CYTOLOGY BRUSHES, by Medical Packaging Corp.

FDA 510(k) K864323, CYTOLOGY BRUSHES, by Medical Packaging Corp.

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Device Classification Name: Spatula, Cervical, Cytological
510(k) Number: K864323
Device Name: CYTOLOGY BRUSHES
Applicant: Medical Packaging Corp.
Regulation Number: 884.4530
Classification Product Code: HHT
Date Received: 11/03/1986
Decision Date: 01/09/1987
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Obstetrics/Gynecology
510k Review Panel: Obstetrics/Gynecology

Total number of pages: 21
Fully redacted pages: 0
Content pages: 21

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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