CLINIX VP 4 TABLE
K-Number: K940721 · 1994-05-03
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Device Summary
Frequently Asked Questions
What is the CLINIX VP 4 TABLE?
CLINIX VP 4 TABLE is a medical device that received FDA 510(k) clearance on 1994-05-03. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K940721.
When did CLINIX VP 4 TABLE receive FDA 510(k) clearance?
CLINIX VP 4 TABLE received FDA 510(k) clearance on 1994-05-03, under 510(k) number K940721.
Who is the listed applicant for CLINIX VP 4 TABLE?
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 CLINIX VP 4 TABLE?
The FDA product code for CLINIX VP 4 TABLE is IXR.
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 (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: IXR)
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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