FDA 510(k)

ID-TAB

K-Number: K913160 · 1991-09-06

Decision Date1991-09-06

Product CodeEGZ

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

ID-TAB is the device name listed in this FDA 510(k) record. The listed applicant is Nix Co. , Ltd.. It received FDA 510(k) clearance on 1991-09-06 under 510(k) number K913160. The device is classified under product code EGZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ID-TAB?

ID-TAB is a medical device that received FDA 510(k) clearance on 1991-09-06. The listed applicant is Nix Co. , Ltd.. The 510(k) number is K913160.

When did ID-TAB receive FDA 510(k) clearance?

ID-TAB received FDA 510(k) clearance on 1991-09-06, under 510(k) number K913160.

Who is the listed applicant for ID-TAB?

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

What is the FDA product code for ID-TAB?

The FDA product code for ID-TAB is EGZ.

Other records listing Nix Co. , Ltd. 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.

K913168SALIBAG

Related Devices (Code: EGZ)

K913168SALIBAGNix Co. , Ltd.K890355DENTAL X-RAY BITE BLOCKBite-A-Block K853451TROLL-BITETrollplast, Inc.K852170EZX YELLOW, BLUE OR ORANGEStrong Marketing K853005S.S. WHITE DENTAL X-RAY FILM HOLDER & ALIGNING ARMThe S. S. White Co.K813378UNI-BITE DENTAL X-RAY FILM HOLDERRinn Corp.

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.