FDA 510(k)

PHILIPS BV 300 SERIES

K-Number: K953910 · 1995-10-18

ApplicantPhilips Medical Systems North America, Inc.

Decision Date1995-10-18

Product CodeOXO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

PHILIPS BV 300 SERIES 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 1995-10-18 under 510(k) number K953910. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS BV 300 SERIES?

PHILIPS BV 300 SERIES is a medical device that received FDA 510(k) clearance on 1995-10-18. The listed applicant is Philips Medical Systems North America, Inc.. The 510(k) number is K953910.

When did PHILIPS BV 300 SERIES receive FDA 510(k) clearance?

PHILIPS BV 300 SERIES received FDA 510(k) clearance on 1995-10-18, under 510(k) number K953910.

Who is the listed applicant for PHILIPS BV 300 SERIES?

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 BV 300 SERIES?

The FDA product code for PHILIPS BV 300 SERIES is OXO.

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

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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.