FV-RF
K-Number: K984111 · 1998-12-11
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Device Summary
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.
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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