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FDA 510(k)

IMMOBILIZING VACUUM MATRESS (IVM)

K-Number: K863511 · 1986-09-25

Decision Date1986-09-25
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IMMOBILIZING VACUUM MATRESS (IVM) is the device name listed in this FDA 510(k) record. The listed applicant is Omnium Services Partners, Inc.. It received FDA 510(k) clearance on 1986-09-25 under 510(k) number K863511. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMMOBILIZING VACUUM MATRESS (IVM)?

IMMOBILIZING VACUUM MATRESS (IVM) is a medical device that received FDA 510(k) clearance on 1986-09-25. The listed applicant is Omnium Services Partners, Inc.. The 510(k) number is K863511.

When did IMMOBILIZING VACUUM MATRESS (IVM) receive FDA 510(k) clearance?

IMMOBILIZING VACUUM MATRESS (IVM) received FDA 510(k) clearance on 1986-09-25, under 510(k) number K863511.

Who is the listed applicant for IMMOBILIZING VACUUM MATRESS (IVM)?

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

What is the FDA product code for IMMOBILIZING VACUUM MATRESS (IVM)?

The FDA product code for IMMOBILIZING VACUUM MATRESS (IVM) is FPP.

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.

Related Devices (Code: FPP)

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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