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FDA 510(k)

BODY WARMER

K-Number: K780426 · 1978-04-27

ApplicantQ-Matic Corp.
Decision Date1978-04-27
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BODY WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Q-Matic Corp.. It received FDA 510(k) clearance on 1978-04-27 under 510(k) number K780426. The device is classified under product code IMD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BODY WARMER?

BODY WARMER is a medical device that received FDA 510(k) clearance on 1978-04-27. The listed applicant is Q-Matic Corp.. The 510(k) number is K780426.

When did BODY WARMER receive FDA 510(k) clearance?

BODY WARMER received FDA 510(k) clearance on 1978-04-27, under 510(k) number K780426.

Who is the listed applicant for BODY WARMER?

The FDA 510(k) record lists Q-Matic Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BODY WARMER?

The FDA product code for BODY WARMER is IMD.

Related Clinical Trials

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Related Devices (Code: IMD)

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.

K221653InfaTherm Disposable Infant Warming MattressInternational BiomedicalK163295Infant Transport Mattress Warmer with DiscRapid Aid Corp.K112547NEO NESTDenovo Proucts, LLCK082087EYEFEEL OPHTHALMIC WARMERBio-Lipid, Inc.K071710BENGAY (R) HEAT THERAPY, PAIN RELIEVING PATCHES/PADS (VARIOUS)Johnson & Johnson Consumer Products, Inc.K021843EYEFEEL OPHTHALMIC WARMERBio-Lipid, 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.

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