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FDA 510(k)

CERVICAL BIOPSY INSTRUMENT

K-Number: K883867 · 1988-11-29

ApplicantMend Technologies, Inc.
Decision Date1988-11-29
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CERVICAL BIOPSY INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Mend Technologies, Inc.. It received FDA 510(k) clearance on 1988-11-29 under 510(k) number K883867. The device is classified under product code HEB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERVICAL BIOPSY INSTRUMENT?

CERVICAL BIOPSY INSTRUMENT is a medical device that received FDA 510(k) clearance on 1988-11-29. The listed applicant is Mend Technologies, Inc.. The 510(k) number is K883867.

When did CERVICAL BIOPSY INSTRUMENT receive FDA 510(k) clearance?

CERVICAL BIOPSY INSTRUMENT received FDA 510(k) clearance on 1988-11-29, under 510(k) number K883867.

Who is the listed applicant for CERVICAL BIOPSY INSTRUMENT?

The FDA 510(k) record lists Mend Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERVICAL BIOPSY INSTRUMENT?

The FDA product code for CERVICAL BIOPSY INSTRUMENT is HEB.

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Other records listing Mend Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K924094MEND APCK884558IOP ADJUSTABLE STIRRUP

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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