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FDA 510(k)

SCR WRAP

K-Number: K822931 · 1982-10-26

Decision Date1982-10-26
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SCR WRAP is the device name listed in this FDA 510(k) record. The listed applicant is Fox Converting, Inc.. It received FDA 510(k) clearance on 1982-10-26 under 510(k) number K822931. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCR WRAP?

SCR WRAP is a medical device that received FDA 510(k) clearance on 1982-10-26. The listed applicant is Fox Converting, Inc.. The 510(k) number is K822931.

When did SCR WRAP receive FDA 510(k) clearance?

SCR WRAP received FDA 510(k) clearance on 1982-10-26, under 510(k) number K822931.

Who is the listed applicant for SCR WRAP?

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

What is the FDA product code for SCR WRAP?

The FDA product code for SCR WRAP is FRG.

Related Devices (Code: FRG)

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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