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FDA 510(k)

FORCEPS & HAMOSTATS

K-Number: K844062 · 1985-01-18

ApplicantI M, Inc.
Decision Date1985-01-18
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCEPS & HAMOSTATS is the device name listed in this FDA 510(k) record. The listed applicant is I M, Inc.. It received FDA 510(k) clearance on 1985-01-18 under 510(k) number K844062. 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 FORCEPS & HAMOSTATS?

FORCEPS & HAMOSTATS is a medical device that received FDA 510(k) clearance on 1985-01-18. The listed applicant is I M, Inc.. The 510(k) number is K844062.

When did FORCEPS & HAMOSTATS receive FDA 510(k) clearance?

FORCEPS & HAMOSTATS received FDA 510(k) clearance on 1985-01-18, under 510(k) number K844062.

Who is the listed applicant for FORCEPS & HAMOSTATS?

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

What is the FDA product code for FORCEPS & HAMOSTATS?

The FDA product code for FORCEPS & HAMOSTATS is GEN.

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Other records listing I M, 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.

K914600NEUROLOGICAL SPONGEK892389BIOPSY KITK881363SYRINGE PREFILLED WITH WATERK880753UMBILICAL CORD CLAMPK872741NUTRIPUMPK871495BANDAGES CATALOG NUMBER: 101 TO 220

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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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