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FDA 510(k)

READY-HEAT BLANKET

K-Number: K042145 · 2004-09-17

ApplicantTechtrade, LLC
Decision Date2004-09-17
Product CodeKME
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

READY-HEAT BLANKET is the device name listed in this FDA 510(k) record. The listed applicant is Techtrade, LLC. It received FDA 510(k) clearance on 2004-09-17 under 510(k) number K042145. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the READY-HEAT BLANKET?

READY-HEAT BLANKET is a medical device that received FDA 510(k) clearance on 2004-09-17. The listed applicant is Techtrade, LLC. The 510(k) number is K042145.

When did READY-HEAT BLANKET receive FDA 510(k) clearance?

READY-HEAT BLANKET received FDA 510(k) clearance on 2004-09-17, under 510(k) number K042145.

Who is the listed applicant for READY-HEAT BLANKET?

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

What is the FDA product code for READY-HEAT BLANKET?

The FDA product code for READY-HEAT BLANKET is KME.

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Other records listing Techtrade, LLC 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.

K050097TECHNO-SCOPE VISUAL STETHOSCOPE

Related Devices (Code: KME)

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.

K944953OREX MEDICAL BEDDINGThantex Specialties, Inc.K933636DISPOSE-A-SHEETBelmac Healthcare Corp.K932539DOCTOR DOWN --RESCUE WRAPThree Dog DownK922143AMERICAN BURN SHEETAmerican Silk Sutures, Inc.K915303FOIL BABY BUNTINGGam Industries, Inc.K912257CHEM-SLEEVE BHaz-Med, Inc.

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.

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