RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLE
K-Number: K943926 · 1994-11-28
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Device Summary
Frequently Asked Questions
What is the RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLE?
RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLE is a medical device that received FDA 510(k) clearance on 1994-11-28. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K943926.
When did RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLE receive FDA 510(k) clearance?
RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLE received FDA 510(k) clearance on 1994-11-28, under 510(k) number K943926.
Who is the listed applicant for RAPIDO 2000 AUTOMATIC RADIOGRAPHIC 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 RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLE?
The FDA product code for RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLE is IZZ.
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: IZZ)
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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