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FDA 510(k)

LOW DOSE SERVOCHEST

K-Number: K810797 · 1981-04-14

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1981-04-14
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LOW DOSE SERVOCHEST 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 1981-04-14 under 510(k) number K810797. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOW DOSE SERVOCHEST?

LOW DOSE SERVOCHEST is a medical device that received FDA 510(k) clearance on 1981-04-14. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K810797.

When did LOW DOSE SERVOCHEST receive FDA 510(k) clearance?

LOW DOSE SERVOCHEST received FDA 510(k) clearance on 1981-04-14, under 510(k) number K810797.

Who is the listed applicant for LOW DOSE SERVOCHEST?

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 LOW DOSE SERVOCHEST?

The FDA product code for LOW DOSE SERVOCHEST is KPR.

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Related Devices (Code: KPR)

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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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