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FDA 510(k)

PHILIPS BV300 SERIES RELEASE 2.1

K-Number: K982706 · 1998-09-02

Decision Date1998-09-02
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS BV300 SERIES RELEASE 2.1 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems, Inc.. It received FDA 510(k) clearance on 1998-09-02 under 510(k) number K982706. 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 BV300 SERIES RELEASE 2.1?

PHILIPS BV300 SERIES RELEASE 2.1 is a medical device that received FDA 510(k) clearance on 1998-09-02. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K982706.

When did PHILIPS BV300 SERIES RELEASE 2.1 receive FDA 510(k) clearance?

PHILIPS BV300 SERIES RELEASE 2.1 received FDA 510(k) clearance on 1998-09-02, under 510(k) number K982706.

Who is the listed applicant for PHILIPS BV300 SERIES RELEASE 2.1?

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

What is the FDA product code for PHILIPS BV300 SERIES RELEASE 2.1?

The FDA product code for PHILIPS BV300 SERIES RELEASE 2.1 is OXO.

Related Clinical Trials

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.

Other records listing Philips Medical Systems, 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.

View all 111 devices →

Related Devices (Code: OXO)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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