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FDA 510(k)

CONSOLE, MOBILE FOR 3 PUMPS W/MASTS

K-Number: K770002 · 1977-03-07

ApplicantCobe Laboratories, Inc.
Decision Date1977-03-07
Product CodeDTQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONSOLE, MOBILE FOR 3 PUMPS W/MASTS is the device name listed in this FDA 510(k) record. The listed applicant is Cobe Laboratories, Inc.. It received FDA 510(k) clearance on 1977-03-07 under 510(k) number K770002. The device is classified under product code DTQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSOLE, MOBILE FOR 3 PUMPS W/MASTS?

CONSOLE, MOBILE FOR 3 PUMPS W/MASTS is a medical device that received FDA 510(k) clearance on 1977-03-07. The listed applicant is Cobe Laboratories, Inc.. The 510(k) number is K770002.

When did CONSOLE, MOBILE FOR 3 PUMPS W/MASTS receive FDA 510(k) clearance?

CONSOLE, MOBILE FOR 3 PUMPS W/MASTS received FDA 510(k) clearance on 1977-03-07, under 510(k) number K770002.

Who is the listed applicant for CONSOLE, MOBILE FOR 3 PUMPS W/MASTS?

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

What is the FDA product code for CONSOLE, MOBILE FOR 3 PUMPS W/MASTS?

The FDA product code for CONSOLE, MOBILE FOR 3 PUMPS W/MASTS is DTQ.

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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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