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FDA 510(k)

IMAGE POST-PROCESSING TECHNIQUES

K-Number: K980831 · 1998-08-27

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1998-08-27
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGE POST-PROCESSING TECHNIQUES 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 1998-08-27 under 510(k) number K980831. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAGE POST-PROCESSING TECHNIQUES?

IMAGE POST-PROCESSING TECHNIQUES is a medical device that received FDA 510(k) clearance on 1998-08-27. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K980831.

When did IMAGE POST-PROCESSING TECHNIQUES receive FDA 510(k) clearance?

IMAGE POST-PROCESSING TECHNIQUES received FDA 510(k) clearance on 1998-08-27, under 510(k) number K980831.

Who is the listed applicant for IMAGE POST-PROCESSING TECHNIQUES?

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 IMAGE POST-PROCESSING TECHNIQUES?

The FDA product code for IMAGE POST-PROCESSING TECHNIQUES is LNH.

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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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