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FDA 510(k)

DISPOSABLE GRASPING FORCEPS

K-Number: K822491 · 1982-09-17

ApplicantVan-Tec, Inc.
Decision Date1982-09-17
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE GRASPING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Van-Tec, Inc.. It received FDA 510(k) clearance on 1982-09-17 under 510(k) number K822491. 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 DISPOSABLE GRASPING FORCEPS?

DISPOSABLE GRASPING FORCEPS is a medical device that received FDA 510(k) clearance on 1982-09-17. The listed applicant is Van-Tec, Inc.. The 510(k) number is K822491.

When did DISPOSABLE GRASPING FORCEPS receive FDA 510(k) clearance?

DISPOSABLE GRASPING FORCEPS received FDA 510(k) clearance on 1982-09-17, under 510(k) number K822491.

Who is the listed applicant for DISPOSABLE GRASPING FORCEPS?

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

What is the FDA product code for DISPOSABLE GRASPING FORCEPS?

The FDA product code for DISPOSABLE GRASPING FORCEPS is GEN.

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Other records listing Van-Tec, 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.

K880096VAN-TEC ASPIRATION BIOPSY SYSTEM W/COLLECTION CUPK880095BERGER PROSTATE CULTURE CYTOLOGY BRUSHK880098VAN-TEC AUTO BIOPSY NEEDLEK880099VAN-TEC BLADDER EVACUATORK880094VAN-TEC ENDOPYELOTOMY KNIFEK874112VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER

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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.K900951GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIPSolos 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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