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FDA 510(k)

CAM-WRAP

K-Number: K810292 · 1981-03-04

ApplicantMedline Industries, Inc.
Decision Date1981-03-04
Product CodeFTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CAM-WRAP is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1981-03-04 under 510(k) number K810292. The device is classified under product code FTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAM-WRAP?

CAM-WRAP is a medical device that received FDA 510(k) clearance on 1981-03-04. The listed applicant is Medline Industries, Inc.. The 510(k) number is K810292.

When did CAM-WRAP receive FDA 510(k) clearance?

CAM-WRAP received FDA 510(k) clearance on 1981-03-04, under 510(k) number K810292.

Who is the listed applicant for CAM-WRAP?

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

What is the FDA product code for CAM-WRAP?

The FDA product code for CAM-WRAP is FTA.

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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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