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FDA 510(k)

MONAGHAN RVM, MODEL 760 OR MODEL 761

K-Number: K853047 · 1985-11-18

ApplicantMonaghan Medical Corp.
Decision Date1985-11-18
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MONAGHAN RVM, MODEL 760 OR MODEL 761 is the device name listed in this FDA 510(k) record. The listed applicant is Monaghan Medical Corp.. It received FDA 510(k) clearance on 1985-11-18 under 510(k) number K853047. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONAGHAN RVM, MODEL 760 OR MODEL 761?

MONAGHAN RVM, MODEL 760 OR MODEL 761 is a medical device that received FDA 510(k) clearance on 1985-11-18. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K853047.

When did MONAGHAN RVM, MODEL 760 OR MODEL 761 receive FDA 510(k) clearance?

MONAGHAN RVM, MODEL 760 OR MODEL 761 received FDA 510(k) clearance on 1985-11-18, under 510(k) number K853047.

Who is the listed applicant for MONAGHAN RVM, MODEL 760 OR MODEL 761?

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

What is the FDA product code for MONAGHAN RVM, MODEL 760 OR MODEL 761?

The FDA product code for MONAGHAN RVM, MODEL 760 OR MODEL 761 is BZQ.

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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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