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FDA 510(k)

SUTURE REMOVING FORCEPS

K-Number: K932385 · 1993-08-06

ApplicantRocket of London, Ltd.
Decision Date1993-08-06
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUTURE REMOVING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Rocket of London, Ltd.. It received FDA 510(k) clearance on 1993-08-06 under 510(k) number K932385. 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 SUTURE REMOVING FORCEPS?

SUTURE REMOVING FORCEPS is a medical device that received FDA 510(k) clearance on 1993-08-06. The listed applicant is Rocket of London, Ltd.. The 510(k) number is K932385.

When did SUTURE REMOVING FORCEPS receive FDA 510(k) clearance?

SUTURE REMOVING FORCEPS received FDA 510(k) clearance on 1993-08-06, under 510(k) number K932385.

Who is the listed applicant for SUTURE REMOVING FORCEPS?

The FDA 510(k) record lists Rocket of London, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUTURE REMOVING FORCEPS?

The FDA product code for SUTURE REMOVING FORCEPS is GEN.

Related Clinical Trials

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Other records listing Rocket of London, Ltd. 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.

K943801URIGLOW TRANSILLUMINATING URETERIC STENT MODELK935665INTRAUTERINE SOUND

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.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900952GS-1200 GRASPING/EXTRACTING FORCEP, 10MMSolos Endoscopy, Inc.K900951GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIPSolos 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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