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FDA 510(k)

COM-MED O.R. TOWEL - NON-STERILE, BLUE, GREEN, WHITE

K-Number: K002691 · 2000-12-08

ApplicantCom-Med International, Inc.
Decision Date2000-12-08
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COM-MED O.R. TOWEL - NON-STERILE, BLUE, GREEN, WHITE is the device name listed in this FDA 510(k) record. The listed applicant is Com-Med International, Inc.. It received FDA 510(k) clearance on 2000-12-08 under 510(k) number K002691. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COM-MED O.R. TOWEL - NON-STERILE, BLUE, GREEN, WHITE?

COM-MED O.R. TOWEL - NON-STERILE, BLUE, GREEN, WHITE is a medical device that received FDA 510(k) clearance on 2000-12-08. The listed applicant is Com-Med International, Inc.. The 510(k) number is K002691.

When did COM-MED O.R. TOWEL - NON-STERILE, BLUE, GREEN, WHITE receive FDA 510(k) clearance?

COM-MED O.R. TOWEL - NON-STERILE, BLUE, GREEN, WHITE received FDA 510(k) clearance on 2000-12-08, under 510(k) number K002691.

Who is the listed applicant for COM-MED O.R. TOWEL - NON-STERILE, BLUE, GREEN, WHITE?

The FDA 510(k) record lists Com-Med International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COM-MED O.R. TOWEL - NON-STERILE, BLUE, GREEN, WHITE?

The FDA product code for COM-MED O.R. TOWEL - NON-STERILE, BLUE, GREEN, WHITE is KKX.

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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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