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FDA 510(k)

BAIR HUGGER(R) PATIENT WARMING SYSTEM-MODIFICATION

K-Number: K903360 · 1990-08-14

Decision Date1990-08-14
Product CodeDWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BAIR HUGGER(R) PATIENT WARMING SYSTEM-MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Augustine Medical, Inc.. It received FDA 510(k) clearance on 1990-08-14 under 510(k) number K903360. 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 BAIR HUGGER(R) PATIENT WARMING SYSTEM-MODIFICATION?

BAIR HUGGER(R) PATIENT WARMING SYSTEM-MODIFICATION is a medical device that received FDA 510(k) clearance on 1990-08-14. The listed applicant is Augustine Medical, Inc.. The 510(k) number is K903360.

When did BAIR HUGGER(R) PATIENT WARMING SYSTEM-MODIFICATION receive FDA 510(k) clearance?

BAIR HUGGER(R) PATIENT WARMING SYSTEM-MODIFICATION received FDA 510(k) clearance on 1990-08-14, under 510(k) number K903360.

Who is the listed applicant for BAIR HUGGER(R) PATIENT WARMING SYSTEM-MODIFICATION?

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

What is the FDA product code for BAIR HUGGER(R) PATIENT WARMING SYSTEM-MODIFICATION?

The FDA product code for BAIR HUGGER(R) PATIENT WARMING SYSTEM-MODIFICATION 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 Augustine Medical, 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 25 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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