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FDA 510(k)

MONITORING KIT, CENTRAL VENOUS PRESSURE

K-Number: K770290 · 1977-03-15

ApplicantArgon Medical Corp.
Decision Date1977-03-15
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MONITORING KIT, CENTRAL VENOUS PRESSURE is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Corp.. It received FDA 510(k) clearance on 1977-03-15 under 510(k) number K770290. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITORING KIT, CENTRAL VENOUS PRESSURE?

MONITORING KIT, CENTRAL VENOUS PRESSURE is a medical device that received FDA 510(k) clearance on 1977-03-15. The listed applicant is Argon Medical Corp.. The 510(k) number is K770290.

When did MONITORING KIT, CENTRAL VENOUS PRESSURE receive FDA 510(k) clearance?

MONITORING KIT, CENTRAL VENOUS PRESSURE received FDA 510(k) clearance on 1977-03-15, under 510(k) number K770290.

Who is the listed applicant for MONITORING KIT, CENTRAL VENOUS PRESSURE?

The FDA 510(k) record lists Argon Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONITORING KIT, CENTRAL VENOUS PRESSURE?

The FDA product code for MONITORING KIT, CENTRAL VENOUS PRESSURE is DQO.

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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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