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FDA 510(k)

JPACS

K-Number: K980918 · 1998-06-03

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1998-06-03
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

JPACS 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 1998-06-03 under 510(k) number K980918. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JPACS?

JPACS is a medical device that received FDA 510(k) clearance on 1998-06-03. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K980918.

When did JPACS receive FDA 510(k) clearance?

JPACS received FDA 510(k) clearance on 1998-06-03, under 510(k) number K980918.

Who is the listed applicant for JPACS?

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 JPACS?

The FDA product code for JPACS is LMD.

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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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