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FDA 510(k)

ALLEGIANCE PORTA-WARM MATTRESS

K-Number: K982652 · 1999-01-21

Decision Date1999-01-21
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ALLEGIANCE PORTA-WARM MATTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Allegiance Healthcare Corp.. It received FDA 510(k) clearance on 1999-01-21 under 510(k) number K982652. 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 ALLEGIANCE PORTA-WARM MATTRESS?

ALLEGIANCE PORTA-WARM MATTRESS is a medical device that received FDA 510(k) clearance on 1999-01-21. The listed applicant is Allegiance Healthcare Corp.. The 510(k) number is K982652.

When did ALLEGIANCE PORTA-WARM MATTRESS receive FDA 510(k) clearance?

ALLEGIANCE PORTA-WARM MATTRESS received FDA 510(k) clearance on 1999-01-21, under 510(k) number K982652.

Who is the listed applicant for ALLEGIANCE PORTA-WARM MATTRESS?

The FDA 510(k) record lists Allegiance Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALLEGIANCE PORTA-WARM MATTRESS?

The FDA product code for ALLEGIANCE PORTA-WARM MATTRESS 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.

Other records listing Allegiance Healthcare Corp. 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 63 devices →

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.

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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