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FDA 510(k)

ORTHO WRAP

K-Number: K830622 · 1983-06-20

ApplicantFast Wrap Co., Inc.
Decision Date1983-06-20
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ORTHO WRAP is the device name listed in this FDA 510(k) record. The listed applicant is Fast Wrap Co., Inc.. It received FDA 510(k) clearance on 1983-06-20 under 510(k) number K830622. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHO WRAP?

ORTHO WRAP is a medical device that received FDA 510(k) clearance on 1983-06-20. The listed applicant is Fast Wrap Co., Inc.. The 510(k) number is K830622.

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

ORTHO WRAP received FDA 510(k) clearance on 1983-06-20, under 510(k) number K830622.

Who is the listed applicant for ORTHO WRAP?

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

What is the FDA product code for ORTHO WRAP?

The FDA product code for ORTHO WRAP is FQM.

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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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