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FDA 510(k)

CATHDAMP

K-Number: K810661 · 1981-03-27

ApplicantMedline Industries, Inc.
Decision Date1981-03-27
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CATHDAMP 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 1981-03-27 under 510(k) number K810661. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHDAMP?

CATHDAMP is a medical device that received FDA 510(k) clearance on 1981-03-27. The listed applicant is Medline Industries, Inc.. The 510(k) number is K810661.

When did CATHDAMP receive FDA 510(k) clearance?

CATHDAMP received FDA 510(k) clearance on 1981-03-27, under 510(k) number K810661.

Who is the listed applicant for CATHDAMP?

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 CATHDAMP?

The FDA product code for CATHDAMP is DRS.

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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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