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FDA 510(k)

UNIVERSAL SLING, SLING & SWATHE

K-Number: K823162 · 1982-11-10

Decision Date1982-11-10
Product CodeILI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL SLING, SLING & SWATHE is the device name listed in this FDA 510(k) record. The listed applicant is Warm & Form, Orthopedic Materials. It received FDA 510(k) clearance on 1982-11-10 under 510(k) number K823162. The device is classified under product code ILI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL SLING, SLING & SWATHE?

UNIVERSAL SLING, SLING & SWATHE is a medical device that received FDA 510(k) clearance on 1982-11-10. The listed applicant is Warm & Form, Orthopedic Materials. The 510(k) number is K823162.

When did UNIVERSAL SLING, SLING & SWATHE receive FDA 510(k) clearance?

UNIVERSAL SLING, SLING & SWATHE received FDA 510(k) clearance on 1982-11-10, under 510(k) number K823162.

Who is the listed applicant for UNIVERSAL SLING, SLING & SWATHE?

The FDA 510(k) record lists Warm & Form, Orthopedic Materials as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIVERSAL SLING, SLING & SWATHE?

The FDA product code for UNIVERSAL SLING, SLING & SWATHE is ILI.

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 Warm & Form, Orthopedic Materials 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 24 devices →

Related Devices (Code: ILI)

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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