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FDA 510(k)

MICROVIEW

K-Number: K790489 · 1979-04-23

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1979-04-23
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MICROVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790489. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROVIEW?

MICROVIEW is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K790489.

When did MICROVIEW receive FDA 510(k) clearance?

MICROVIEW received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790489.

Who is the listed applicant for MICROVIEW?

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

What is the FDA product code for MICROVIEW?

The FDA product code for MICROVIEW is IYO.

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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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