FDA 510(k)

A2J MZ 44 B TYPE

K-Number: K880981 · 1988-04-22

Decision Date1988-04-22

Product CodeIWE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

A2J MZ 44 B TYPE is the device name listed in this FDA 510(k) record. The listed applicant is A2j, Inc.. It received FDA 510(k) clearance on 1988-04-22 under 510(k) number K880981. 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 A2J MZ 44 B TYPE?

A2J MZ 44 B TYPE is a medical device that received FDA 510(k) clearance on 1988-04-22. The listed applicant is A2j, Inc.. The 510(k) number is K880981.

When did A2J MZ 44 B TYPE receive FDA 510(k) clearance?

A2J MZ 44 B TYPE received FDA 510(k) clearance on 1988-04-22, under 510(k) number K880981.

Who is the listed applicant for A2J MZ 44 B TYPE?

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 A2J MZ 44 B TYPE?

The FDA product code for A2J MZ 44 B TYPE 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.

K931974AZ 92 K904127A2J TELEMETER K881591A2J MZ 45 LASER LIGHT FOR POSITIONING

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.