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FDA 510(k)

HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES

K-Number: K844880 · 1985-01-25

ApplicantHuntleigh Technology, Inc.
Decision Date1985-01-25
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Technology, Inc.. It received FDA 510(k) clearance on 1985-01-25 under 510(k) number K844880. 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 HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES?

HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES is a medical device that received FDA 510(k) clearance on 1985-01-25. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K844880.

When did HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES receive FDA 510(k) clearance?

HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES received FDA 510(k) clearance on 1985-01-25, under 510(k) number K844880.

Who is the listed applicant for HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES?

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

What is the FDA product code for HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES?

The FDA product code for HUNTLEIGH AIR-O-PAD AOP1 ALTERNATING PRESS-MATTRES is FNM.

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Other records listing Huntleigh Technology, Inc. as applicant

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Related Devices (Code: FNM)

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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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