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FDA 510(k)

CONPHAR ALLIS FORCEPS

K-Number: K821353 · 1982-05-27

ApplicantConphar, Inc.
Decision Date1982-05-27
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONPHAR ALLIS FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-05-27 under 510(k) number K821353. 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 CONPHAR ALLIS FORCEPS?

CONPHAR ALLIS FORCEPS is a medical device that received FDA 510(k) clearance on 1982-05-27. The listed applicant is Conphar, Inc.. The 510(k) number is K821353.

When did CONPHAR ALLIS FORCEPS receive FDA 510(k) clearance?

CONPHAR ALLIS FORCEPS received FDA 510(k) clearance on 1982-05-27, under 510(k) number K821353.

Who is the listed applicant for CONPHAR ALLIS FORCEPS?

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

What is the FDA product code for CONPHAR ALLIS FORCEPS?

The FDA product code for CONPHAR ALLIS FORCEPS is GEN.

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Other records listing Conphar, 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.

K821825CONPHAR SILICONE FEEDING TUBEK821295OLSEN HEGAR NEEDLE HOLDERSK821289MAYO-HEGAR NEEDLE HOLDERK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2

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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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