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FDA 510(k)

RECOVER ADULT VEIN WARMER

K-Number: K963689 · 1996-12-12

ApplicantFlorida Medical Industries, Inc.
Decision Date1996-12-12
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RECOVER ADULT VEIN WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Florida Medical Industries, Inc.. It received FDA 510(k) clearance on 1996-12-12 under 510(k) number K963689. 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 RECOVER ADULT VEIN WARMER?

RECOVER ADULT VEIN WARMER is a medical device that received FDA 510(k) clearance on 1996-12-12. The listed applicant is Florida Medical Industries, Inc.. The 510(k) number is K963689.

When did RECOVER ADULT VEIN WARMER receive FDA 510(k) clearance?

RECOVER ADULT VEIN WARMER received FDA 510(k) clearance on 1996-12-12, under 510(k) number K963689.

Who is the listed applicant for RECOVER ADULT VEIN WARMER?

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

What is the FDA product code for RECOVER ADULT VEIN WARMER?

The FDA product code for RECOVER ADULT VEIN WARMER is IMD.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Florida Medical Industries, 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.

K964523RECOVER INFANT HEEL WARMER (5100)

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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