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FDA 510(k)

15-490 TO 15-520 VARIOUS SPLINTER FORCEPS PEET, ST

K-Number: K851771 · 1985-06-20

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

Device Summary

15-490 TO 15-520 VARIOUS SPLINTER FORCEPS PEET, ST 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 K851771. 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 15-490 TO 15-520 VARIOUS SPLINTER FORCEPS PEET, ST?

15-490 TO 15-520 VARIOUS SPLINTER FORCEPS PEET, ST is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851771.

When did 15-490 TO 15-520 VARIOUS SPLINTER FORCEPS PEET, ST receive FDA 510(k) clearance?

15-490 TO 15-520 VARIOUS SPLINTER FORCEPS PEET, ST received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851771.

Who is the listed applicant for 15-490 TO 15-520 VARIOUS SPLINTER FORCEPS PEET, ST?

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 15-490 TO 15-520 VARIOUS SPLINTER FORCEPS PEET, ST?

The FDA product code for 15-490 TO 15-520 VARIOUS SPLINTER FORCEPS PEET, ST 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, WOLFK8517191070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERSK8517272020-1/2 TO 2220 VARIOUS DENTAL WAX & MODELLING CAK851718930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTESK8517201155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS

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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