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FDA 510(k)

SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000

K-Number: K040632 · 2004-04-27

Decision Date2004-04-27
Product CodeDWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000 is the device name listed in this FDA 510(k) record. The listed applicant is Smiths Medical Asd, Inc.. It received FDA 510(k) clearance on 2004-04-27 under 510(k) number K040632. The device is classified under product code DWJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000?

SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000 is a medical device that received FDA 510(k) clearance on 2004-04-27. The listed applicant is Smiths Medical Asd, Inc.. The 510(k) number is K040632.

When did SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000 receive FDA 510(k) clearance?

SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000 received FDA 510(k) clearance on 2004-04-27, under 510(k) number K040632.

Who is the listed applicant for SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000?

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

What is the FDA product code for SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000?

The FDA product code for SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000 is DWJ.

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.

Other records listing Smiths Medical Asd, 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.

View all 51 devices →

Related Devices (Code: DWJ)

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.

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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