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FDA 510(k)

SKIL-CARE TURN AND HOLD PAD

K-Number: K792318 · 1979-12-20

Decision Date1979-12-20
Product CodeFMR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SKIL-CARE TURN AND HOLD PAD is the device name listed in this FDA 510(k) record. The listed applicant is Skil-Care Corp.. It received FDA 510(k) clearance on 1979-12-20 under 510(k) number K792318. The device is classified under product code FMR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKIL-CARE TURN AND HOLD PAD?

SKIL-CARE TURN AND HOLD PAD is a medical device that received FDA 510(k) clearance on 1979-12-20. The listed applicant is Skil-Care Corp.. The 510(k) number is K792318.

When did SKIL-CARE TURN AND HOLD PAD receive FDA 510(k) clearance?

SKIL-CARE TURN AND HOLD PAD received FDA 510(k) clearance on 1979-12-20, under 510(k) number K792318.

Who is the listed applicant for SKIL-CARE TURN AND HOLD PAD?

The FDA 510(k) record lists Skil-Care Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKIL-CARE TURN AND HOLD PAD?

The FDA product code for SKIL-CARE TURN AND HOLD PAD is FMR.

Other records listing Skil-Care 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.

View all 20 devices →

Related Devices (Code: FMR)

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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