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FDA 510(k)

MATTRESS, AIR FLOATATION, ALTERN. PRESS.

K-Number: K803307 · 1981-01-13

Decision Date1981-01-13
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MATTRESS, AIR FLOATATION, ALTERN. PRESS. is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical Equipment Corp.. It received FDA 510(k) clearance on 1981-01-13 under 510(k) number K803307. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATTRESS, AIR FLOATATION, ALTERN. PRESS.?

MATTRESS, AIR FLOATATION, ALTERN. PRESS. is a medical device that received FDA 510(k) clearance on 1981-01-13. The listed applicant is Intl. Medical Equipment Corp.. The 510(k) number is K803307.

When did MATTRESS, AIR FLOATATION, ALTERN. PRESS. receive FDA 510(k) clearance?

MATTRESS, AIR FLOATATION, ALTERN. PRESS. received FDA 510(k) clearance on 1981-01-13, under 510(k) number K803307.

Who is the listed applicant for MATTRESS, AIR FLOATATION, ALTERN. PRESS.?

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

What is the FDA product code for MATTRESS, AIR FLOATATION, ALTERN. PRESS.?

The FDA product code for MATTRESS, AIR FLOATATION, ALTERN. PRESS. is FNM.

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 Intl. Medical Equipment 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.

Related Devices (Code: FNM)

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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