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FDA 510(k)

LIFE-AIR 1000 PATIENT WARMING COVER

K-Number: K933764 · 1993-11-09

Decision Date1993-11-09
Product CodeDWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFE-AIR 1000 PATIENT WARMING COVER is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Dynamics, Inc.. It received FDA 510(k) clearance on 1993-11-09 under 510(k) number K933764. 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 LIFE-AIR 1000 PATIENT WARMING COVER?

LIFE-AIR 1000 PATIENT WARMING COVER is a medical device that received FDA 510(k) clearance on 1993-11-09. The listed applicant is Progressive Dynamics, Inc.. The 510(k) number is K933764.

When did LIFE-AIR 1000 PATIENT WARMING COVER receive FDA 510(k) clearance?

LIFE-AIR 1000 PATIENT WARMING COVER received FDA 510(k) clearance on 1993-11-09, under 510(k) number K933764.

Who is the listed applicant for LIFE-AIR 1000 PATIENT WARMING COVER?

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

What is the FDA product code for LIFE-AIR 1000 PATIENT WARMING COVER?

The FDA product code for LIFE-AIR 1000 PATIENT WARMING COVER 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 Progressive Dynamics, 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 7 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

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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