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FDA 510(k)

7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1

K-Number: K851751 · 1985-06-20

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

Device Summary

7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1 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 K851751. The device is classified under product code GDX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1?

7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1 is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851751.

When did 7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1 receive FDA 510(k) clearance?

7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1 received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851751.

Who is the listed applicant for 7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1?

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 7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1?

The FDA product code for 7-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1 is GDX.

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: GDX)

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.

K923689SURGISTAR BLADESSurgistar, Inc.K921167ULTRABLADEMicron Technology, Inc.K914086ICAN CYLINDRICAL SPONGESIcn Pharmaceuticals, Inc.K904505CCI CORNEAL SCARIFIERBuckman Co., Inc.K9053801-CUT ACL GRAFT KNIFEDepuy, Inc.K895682VESSEL LOOPSApplied Medical Technologies

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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