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FDA 510(k)

2250/1 TO 2285/2 VARIOUS COTTON TWEEZERS

K-Number: K851728 · 1985-07-01

ApplicantArtiberia
Decision Date1985-07-01
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

2250/1 TO 2285/2 VARIOUS COTTON TWEEZERS is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-07-01 under 510(k) number K851728. 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 2250/1 TO 2285/2 VARIOUS COTTON TWEEZERS?

2250/1 TO 2285/2 VARIOUS COTTON TWEEZERS is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Artiberia. The 510(k) number is K851728.

When did 2250/1 TO 2285/2 VARIOUS COTTON TWEEZERS receive FDA 510(k) clearance?

2250/1 TO 2285/2 VARIOUS COTTON TWEEZERS received FDA 510(k) clearance on 1985-07-01, under 510(k) number K851728.

Who is the listed applicant for 2250/1 TO 2285/2 VARIOUS COTTON TWEEZERS?

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 2250/1 TO 2285/2 VARIOUS COTTON TWEEZERS?

The FDA product code for 2250/1 TO 2285/2 VARIOUS COTTON TWEEZERS 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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