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FDA 510(k)

PHILIPS TOMOSCAN AV-NT

K-Number: K991278 · 1999-05-13

ApplicantPhilips Medical Systems North America, Inc.
Decision Date1999-05-13
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS TOMOSCAN AV-NT is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems North America, Inc.. It received FDA 510(k) clearance on 1999-05-13 under 510(k) number K991278. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS TOMOSCAN AV-NT?

PHILIPS TOMOSCAN AV-NT is a medical device that received FDA 510(k) clearance on 1999-05-13. The listed applicant is Philips Medical Systems North America, Inc.. The 510(k) number is K991278.

When did PHILIPS TOMOSCAN AV-NT receive FDA 510(k) clearance?

PHILIPS TOMOSCAN AV-NT received FDA 510(k) clearance on 1999-05-13, under 510(k) number K991278.

Who is the listed applicant for PHILIPS TOMOSCAN AV-NT?

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

What is the FDA product code for PHILIPS TOMOSCAN AV-NT?

The FDA product code for PHILIPS TOMOSCAN AV-NT is JAK.

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Other records listing Philips Medical Systems North America, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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