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FDA 510(k)

VANCE-AMBROSE RESECTOSCOPE FORCEPS

K-Number: K812785 · 1981-11-16

ApplicantVance Products, Inc.
Decision Date1981-11-16
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VANCE-AMBROSE RESECTOSCOPE FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Vance Products, Inc.. It received FDA 510(k) clearance on 1981-11-16 under 510(k) number K812785. 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 VANCE-AMBROSE RESECTOSCOPE FORCEPS?

VANCE-AMBROSE RESECTOSCOPE FORCEPS is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is Vance Products, Inc.. The 510(k) number is K812785.

When did VANCE-AMBROSE RESECTOSCOPE FORCEPS receive FDA 510(k) clearance?

VANCE-AMBROSE RESECTOSCOPE FORCEPS received FDA 510(k) clearance on 1981-11-16, under 510(k) number K812785.

Who is the listed applicant for VANCE-AMBROSE RESECTOSCOPE FORCEPS?

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

What is the FDA product code for VANCE-AMBROSE RESECTOSCOPE FORCEPS?

The FDA product code for VANCE-AMBROSE RESECTOSCOPE FORCEPS is GEN.

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Other records listing Vance 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.

K820313VPI-FAIR URETHRAL STENTK812995VANCE-JACOBELLIS MICROHEMATURIA CATHETERK813278VPI URETERAL DILATATION BALLON CATHETERK812057VANCE CYSTOSCOPICK811833VNACE FASCIAL DILATOR SETK811454VANCE PROSTATIC ASPIRATION SET

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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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