FDA 510(k)

MEDLINE SUCTION COAGULATOR

K-Number: K122949 · 2013-10-16

Decision Date2013-10-16

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MEDLINE SUCTION COAGULATOR 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 2013-10-16 under 510(k) number K122949. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE SUCTION COAGULATOR?

MEDLINE SUCTION COAGULATOR is a medical device that received FDA 510(k) clearance on 2013-10-16. The listed applicant is Medline Industries, Inc.. The 510(k) number is K122949.

When did MEDLINE SUCTION COAGULATOR receive FDA 510(k) clearance?

MEDLINE SUCTION COAGULATOR received FDA 510(k) clearance on 2013-10-16, under 510(k) number K122949.

Who is the listed applicant for MEDLINE SUCTION COAGULATOR?

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 MEDLINE SUCTION COAGULATOR?

The FDA product code for MEDLINE SUCTION COAGULATOR is GEI.

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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.