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FDA 510(k)

CONPHAR MANOMETER CONNECTORS

K-Number: K792113 · 1979-12-05

ApplicantConphar, Inc.
Decision Date1979-12-05
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONPHAR MANOMETER CONNECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1979-12-05 under 510(k) number K792113. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR MANOMETER CONNECTORS?

CONPHAR MANOMETER CONNECTORS is a medical device that received FDA 510(k) clearance on 1979-12-05. The listed applicant is Conphar, Inc.. The 510(k) number is K792113.

When did CONPHAR MANOMETER CONNECTORS receive FDA 510(k) clearance?

CONPHAR MANOMETER CONNECTORS received FDA 510(k) clearance on 1979-12-05, under 510(k) number K792113.

Who is the listed applicant for CONPHAR MANOMETER CONNECTORS?

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

What is the FDA product code for CONPHAR MANOMETER CONNECTORS?

The FDA product code for CONPHAR MANOMETER CONNECTORS is DTL.

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Other records listing Conphar, Inc. as applicant

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Related Devices (Code: DTL)

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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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