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FDA 510(k)

REUSABLE MONOPOLAR FORCEPS

K-Number: K950877 · 1995-03-09

Decision Date1995-03-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REUSABLE MONOPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Boston Surgical Products, Inc.. It received FDA 510(k) clearance on 1995-03-09 under 510(k) number K950877. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSABLE MONOPOLAR FORCEPS?

REUSABLE MONOPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1995-03-09. The listed applicant is Boston Surgical Products, Inc.. The 510(k) number is K950877.

When did REUSABLE MONOPOLAR FORCEPS receive FDA 510(k) clearance?

REUSABLE MONOPOLAR FORCEPS received FDA 510(k) clearance on 1995-03-09, under 510(k) number K950877.

Who is the listed applicant for REUSABLE MONOPOLAR FORCEPS?

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

What is the FDA product code for REUSABLE MONOPOLAR FORCEPS?

The FDA product code for REUSABLE MONOPOLAR FORCEPS is GEI.

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 Boston Surgical Products, 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.

View all 17 devices →

Related Devices (Code: GEI)

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

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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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