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FDA 510(k)

DISPOS. & SPONGE FORCEPS PEAN ARTERY

K-Number: K843074 · 1984-08-17

ApplicantGreene International Corp.
Decision Date1984-08-17
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOS. & SPONGE FORCEPS PEAN ARTERY is the device name listed in this FDA 510(k) record. The listed applicant is Greene International Corp.. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K843074. 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 DISPOS. & SPONGE FORCEPS PEAN ARTERY?

DISPOS. & SPONGE FORCEPS PEAN ARTERY is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Greene International Corp.. The 510(k) number is K843074.

When did DISPOS. & SPONGE FORCEPS PEAN ARTERY receive FDA 510(k) clearance?

DISPOS. & SPONGE FORCEPS PEAN ARTERY received FDA 510(k) clearance on 1984-08-17, under 510(k) number K843074.

Who is the listed applicant for DISPOS. & SPONGE FORCEPS PEAN ARTERY?

The FDA 510(k) record lists Greene International Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOS. & SPONGE FORCEPS PEAN ARTERY?

The FDA product code for DISPOS. & SPONGE FORCEPS PEAN ARTERY is GEN.

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Other records listing Greene International Corp. 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.

K883827MASKS, VARIOUS TYPES OF SURGICAL MASKSK883828CONE MASKS, VARIOUS TYPES OF SURGICAL CONE MASKSK880484SURGICAL GARMENTSK870617VARIOUS TYES OF SURGICAL GARMENTSK843075UTILITY SCISSORS DISPOSABLE ITEMSK843073FIXED VOL. DISPENSERS, ADJUST VOL-HUNPIP

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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.K900948GS-1002 GRASPING FORCEP, 5MM WITH RATCHETSolos 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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