MATTRESS, AIR FLOATATION, ALTERN. PRESS.
K-Number: K803307 · 1981-01-13
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Device Summary
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
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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