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FDA 510(k)

OVAL CUP BIOPSY FORCEP (MODEL 18/5)

K-Number: K874012 · 1987-12-29

ApplicantEndovations
Decision Date1987-12-29
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OVAL CUP BIOPSY FORCEP (MODEL 18/5) is the device name listed in this FDA 510(k) record. The listed applicant is Endovations. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K874012. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OVAL CUP BIOPSY FORCEP (MODEL 18/5)?

OVAL CUP BIOPSY FORCEP (MODEL 18/5) is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Endovations. The 510(k) number is K874012.

When did OVAL CUP BIOPSY FORCEP (MODEL 18/5) receive FDA 510(k) clearance?

OVAL CUP BIOPSY FORCEP (MODEL 18/5) received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874012.

Who is the listed applicant for OVAL CUP BIOPSY FORCEP (MODEL 18/5)?

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

What is the FDA product code for OVAL CUP BIOPSY FORCEP (MODEL 18/5)?

The FDA product code for OVAL CUP BIOPSY FORCEP (MODEL 18/5) is OCZ.

Related Clinical Trials

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.

Other records listing Endovations 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.

View all 37 devices →

Related Devices (Code: OCZ)

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.

Official Source

View on FDA Database →

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

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