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FDA 510(k)

17-280,17-576 HAEMOSTATIC FORCEPS SPENCERUELLS, KI

K-Number: K851773 · 1985-06-20

ApplicantArtiberia
Decision Date1985-06-20
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

17-280,17-576 HAEMOSTATIC FORCEPS SPENCERUELLS, KI is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-06-20 under 510(k) number K851773. 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 17-280,17-576 HAEMOSTATIC FORCEPS SPENCERUELLS, KI?

17-280,17-576 HAEMOSTATIC FORCEPS SPENCERUELLS, KI is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851773.

When did 17-280,17-576 HAEMOSTATIC FORCEPS SPENCERUELLS, KI receive FDA 510(k) clearance?

17-280,17-576 HAEMOSTATIC FORCEPS SPENCERUELLS, KI received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851773.

Who is the listed applicant for 17-280,17-576 HAEMOSTATIC FORCEPS SPENCERUELLS, KI?

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

What is the FDA product code for 17-280,17-576 HAEMOSTATIC FORCEPS SPENCERUELLS, KI?

The FDA product code for 17-280,17-576 HAEMOSTATIC FORCEPS SPENCERUELLS, KI is GEN.

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Other records listing Artiberia 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.

K8517451-100 UNIVERSAL SET OTOSCOPE & LARYNX EXPLORATON BK85178627-230 TO 27-234 VARIOUS CAST BREAKERS, WOLFK8517272020-1/2 TO 2220 VARIOUS DENTAL WAX & MODELLING CAK851718930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTESK8517201155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORSK8517191070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS

View all 79 devices →

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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