FDA 510(k)

RIA/MAT FPA TEST KIT

K-Number: K884496 · 1988-11-16

Decision Date1988-11-16

Product CodeDAN

Advisory CommitteeIM

DecisionSubstantially Equivalent

Device Summary

RIA/MAT FPA TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Altana, Inc.. It received FDA 510(k) clearance on 1988-11-16 under 510(k) number K884496. The device is classified under product code DAN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA/MAT FPA TEST KIT?

RIA/MAT FPA TEST KIT is a medical device that received FDA 510(k) clearance on 1988-11-16. The listed applicant is Altana, Inc.. The 510(k) number is K884496.

When did RIA/MAT FPA TEST KIT receive FDA 510(k) clearance?

RIA/MAT FPA TEST KIT received FDA 510(k) clearance on 1988-11-16, under 510(k) number K884496.

Who is the listed applicant for RIA/MAT FPA TEST KIT?

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

What is the FDA product code for RIA/MAT FPA TEST KIT?

The FDA product code for RIA/MAT FPA TEST KIT is DAN.

Other records listing Altana, 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.

K934205SEARCH-SONIC

Related Devices (Code: DAN)

K854384ASSERACHROM FPA KITAmerican Bioproducts Co.K821151RIA-QUANT FPA TEST KITMallinckrodt Critical Care

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.