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FDA 510(k)

MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA

K-Number: K904050 · 1990-12-05

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1990-12-05
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA 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 1990-12-05 under 510(k) number K904050. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA?

MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA is a medical device that received FDA 510(k) clearance on 1990-12-05. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K904050.

When did MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA receive FDA 510(k) clearance?

MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA received FDA 510(k) clearance on 1990-12-05, under 510(k) number K904050.

Who is the listed applicant for MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA?

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 MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA?

The FDA product code for MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA is IYX.

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Related Devices (Code: IYX)

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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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