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FDA 510(k)

IMSI/EASY FLOAT MATTRESS

K-Number: K872876 · 1987-10-13

Decision Date1987-10-13
Product CodeFOH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IMSI/EASY FLOAT MATTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Management Services, Inc.. It received FDA 510(k) clearance on 1987-10-13 under 510(k) number K872876. The device is classified under product code FOH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMSI/EASY FLOAT MATTRESS?

IMSI/EASY FLOAT MATTRESS is a medical device that received FDA 510(k) clearance on 1987-10-13. The listed applicant is Intl. Management Services, Inc.. The 510(k) number is K872876.

When did IMSI/EASY FLOAT MATTRESS receive FDA 510(k) clearance?

IMSI/EASY FLOAT MATTRESS received FDA 510(k) clearance on 1987-10-13, under 510(k) number K872876.

Who is the listed applicant for IMSI/EASY FLOAT MATTRESS?

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

What is the FDA product code for IMSI/EASY FLOAT MATTRESS?

The FDA product code for IMSI/EASY FLOAT MATTRESS is FOH.

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. Management Services, 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.

Related Devices (Code: FOH)

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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