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FDA 510(k)

HARTMAN FORCEPS STRAIGHT 3 1/2

K-Number: K821278 · 1982-05-27

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

Device Summary

HARTMAN FORCEPS STRAIGHT 3 1/2 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 K821278. 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 HARTMAN FORCEPS STRAIGHT 3 1/2?

HARTMAN FORCEPS STRAIGHT 3 1/2 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 K821278.

When did HARTMAN FORCEPS STRAIGHT 3 1/2 receive FDA 510(k) clearance?

HARTMAN FORCEPS STRAIGHT 3 1/2 received FDA 510(k) clearance on 1982-05-27, under 510(k) number K821278.

Who is the listed applicant for HARTMAN FORCEPS STRAIGHT 3 1/2?

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 HARTMAN FORCEPS STRAIGHT 3 1/2?

The FDA product code for HARTMAN FORCEPS STRAIGHT 3 1/2 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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