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FDA 510(k)

HEMOSTATIC/TUBE OCCLUDING FORCEPS

K-Number: K800435 · 1980-03-12

ApplicantDravon Medical, Inc.
Decision Date1980-03-12
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEMOSTATIC/TUBE OCCLUDING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Dravon Medical, Inc.. It received FDA 510(k) clearance on 1980-03-12 under 510(k) number K800435. 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 HEMOSTATIC/TUBE OCCLUDING FORCEPS?

HEMOSTATIC/TUBE OCCLUDING FORCEPS is a medical device that received FDA 510(k) clearance on 1980-03-12. The listed applicant is Dravon Medical, Inc.. The 510(k) number is K800435.

When did HEMOSTATIC/TUBE OCCLUDING FORCEPS receive FDA 510(k) clearance?

HEMOSTATIC/TUBE OCCLUDING FORCEPS received FDA 510(k) clearance on 1980-03-12, under 510(k) number K800435.

Who is the listed applicant for HEMOSTATIC/TUBE OCCLUDING FORCEPS?

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

What is the FDA product code for HEMOSTATIC/TUBE OCCLUDING FORCEPS?

The FDA product code for HEMOSTATIC/TUBE OCCLUDING FORCEPS is GEN.

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Other records listing Dravon Medical, 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.

K873455S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSISK860770AM-100 I/A AMPACK832739STEDIFLO INFUSION SETK831842DRAVON T CLAMPK812772PERITONEAL DIALYSIS CYCLER SET (8UNIT)K812771PERITONEAL DIALYSIS DRAINAGE

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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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