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FDA 510(k)

27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF

K-Number: K851786 · 1985-07-09

ApplicantArtiberia
Decision Date1985-07-09
Product CodeLGG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-07-09 under 510(k) number K851786. The device is classified under product code LGG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF?

27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF is a medical device that received FDA 510(k) clearance on 1985-07-09. The listed applicant is Artiberia. The 510(k) number is K851786.

When did 27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF receive FDA 510(k) clearance?

27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF received FDA 510(k) clearance on 1985-07-09, under 510(k) number K851786.

Who is the listed applicant for 27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF?

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 27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF?

The FDA product code for 27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF is LGG.

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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 BK851718930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTESK8517272020-1/2 TO 2220 VARIOUS DENTAL WAX & MODELLING CAK8517191070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERSK8517231300/10 TO 1305/89-92 VARIOUS CUTTING INSTRUMENTSK8517201155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS

View all 79 devices →

Related Devices (Code: LGG)

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.

K870100PLASTER STANDOrthopedic Systems, Inc.K834384MODULAR EXTREMITY CASTING SUPPORTBuckman Co., 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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