SKIL-CARE SUPER-SOFT LIMB RESTRAINTS
K-Number: K792012 · 1979-10-26
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Device Summary
Frequently Asked Questions
What is the SKIL-CARE SUPER-SOFT LIMB RESTRAINTS?
SKIL-CARE SUPER-SOFT LIMB RESTRAINTS is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is Skil-Care Corp.. The 510(k) number is K792012.
When did SKIL-CARE SUPER-SOFT LIMB RESTRAINTS receive FDA 510(k) clearance?
SKIL-CARE SUPER-SOFT LIMB RESTRAINTS received FDA 510(k) clearance on 1979-10-26, under 510(k) number K792012.
Who is the listed applicant for SKIL-CARE SUPER-SOFT LIMB RESTRAINTS?
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 SUPER-SOFT LIMB RESTRAINTS?
The FDA product code for SKIL-CARE SUPER-SOFT LIMB RESTRAINTS is FMQ.
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 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.
Related Devices (Code: FMQ)
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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