FDA 510(k)

READY-BOX BODY-TEMP MEDIA WARMER MALLIN-

K-Number: K823356 · 1982-12-03

Decision Date1982-12-03

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

READY-BOX BODY-TEMP MEDIA WARMER MALLIN- is the device name listed in this FDA 510(k) record. The listed applicant is Forma Scientific, Inc.. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K823356. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the READY-BOX BODY-TEMP MEDIA WARMER MALLIN-?

READY-BOX BODY-TEMP MEDIA WARMER MALLIN- is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Forma Scientific, Inc.. The 510(k) number is K823356.

When did READY-BOX BODY-TEMP MEDIA WARMER MALLIN- receive FDA 510(k) clearance?

READY-BOX BODY-TEMP MEDIA WARMER MALLIN- received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823356.

Who is the listed applicant for READY-BOX BODY-TEMP MEDIA WARMER MALLIN-?

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

What is the FDA product code for READY-BOX BODY-TEMP MEDIA WARMER MALLIN-?

The FDA product code for READY-BOX BODY-TEMP MEDIA WARMER MALLIN- is DXT.

Related Clinical Trials

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.

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Other records listing Forma Scientific, Inc. as applicant

K841631MODEL 3014 SUCTION UNIT K821401MALLINCKRODT DIAG. MEDIA WARMER K812826FORMA CH/P GAS PROCESSOR

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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.