MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLE
K-Number: K932749 · 1993-07-22
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Device Summary
Frequently Asked Questions
What is the MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLE?
MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLE is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Med Mart, Inc.. The 510(k) number is K932749.
When did MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLE receive FDA 510(k) clearance?
MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLE received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932749.
Who is the listed applicant for MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLE?
The FDA 510(k) record lists Med Mart, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLE?
The FDA product code for MODEL M4501,M4502,M4503,M4504,M4505 TILT TABLE is INQ.
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 Med Mart, 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: INQ)
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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