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FDA 510(k)

FV-RF

K-Number: K984111 · 1998-12-11

Decision Date1998-12-11
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FV-RF 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 1998-12-11 under 510(k) number K984111. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FV-RF?

FV-RF is a medical device that received FDA 510(k) clearance on 1998-12-11. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K984111.

When did FV-RF receive FDA 510(k) clearance?

FV-RF received FDA 510(k) clearance on 1998-12-11, under 510(k) number K984111.

Who is the listed applicant for FV-RF?

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 FV-RF?

The FDA product code for FV-RF is KPR.

Other records listing Philips Medical Systems (Cleveland), 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 190 devices →

Related Devices (Code: KPR)

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

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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