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FDA 510(k)

DISPOSABLE BIPOLAR FORCEPS

K-Number: K873978 · 1987-11-23

ApplicantE.M. Adams
Decision Date1987-11-23
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is E.M. Adams. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K873978. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE BIPOLAR FORCEPS?

DISPOSABLE BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is E.M. Adams. The 510(k) number is K873978.

When did DISPOSABLE BIPOLAR FORCEPS receive FDA 510(k) clearance?

DISPOSABLE BIPOLAR FORCEPS received FDA 510(k) clearance on 1987-11-23, under 510(k) number K873978.

Who is the listed applicant for DISPOSABLE BIPOLAR FORCEPS?

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

What is the FDA product code for DISPOSABLE BIPOLAR FORCEPS?

The FDA product code for DISPOSABLE BIPOLAR FORCEPS is GEN.

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Other records listing E.M. Adams 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.

K905173SPLASH GUARDK910468STERILE DISPOSABLE DRAPE(S)K850063INSTRUMENT POCKETK843724I.V. START KIT & OBSTETRICAL KITK843783WET PACKK843782DRY TRAY

View all 21 devices →

Related Devices (Code: GEN)

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.

K031828NATURALASE LP ND:YAG LASERFocus Medical, LLCK953962FORCEPSBiopsys Medical, Inc.K932385SUTURE REMOVING FORCEPSRocket of London, Ltd.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900952GS-1200 GRASPING/EXTRACTING FORCEP, 10MMSolos Endoscopy, Inc.

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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