FDA 510(k)

AZ 92

K-Number: K931974 · 1993-10-08

Decision Date1993-10-08

Product CodeIWE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

AZ 92 is the device name listed in this FDA 510(k) record. The listed applicant is A2j, Inc.. It received FDA 510(k) clearance on 1993-10-08 under 510(k) number K931974. The device is classified under product code IWE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AZ 92?

AZ 92 is a medical device that received FDA 510(k) clearance on 1993-10-08. The listed applicant is A2j, Inc.. The 510(k) number is K931974.

When did AZ 92 receive FDA 510(k) clearance?

AZ 92 received FDA 510(k) clearance on 1993-10-08, under 510(k) number K931974.

Who is the listed applicant for AZ 92?

The FDA 510(k) record lists A2j, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AZ 92?

The FDA product code for AZ 92 is IWE.

Other records listing A2j, Inc. 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.

K904127A2J TELEMETER K881591A2J MZ 45 LASER LIGHT FOR POSITIONING K880981A2J MZ 44 B TYPE

Related Devices (Code: IWE)

K973162DUAL RADIATION TARGETING SYSTEM DRTS DRAPEHogan & Hartson K955236GREEN TEC-2100Medtec, Inc.K954414CENTRALITE BACKPOINTERDiacor, Inc.K950293TEC-2110 GREEN LASER MODEL MT-HNGMedtec, Inc.K950112CENTRALITE(R)-DLL SERIESDiacor, Inc.K951601MED-TEC STRING RETICLE TRAYMedtec, 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.