TREATMENT TABLES, MANUALLY ACTIVATED
K-Number: K931635 · 1993-07-21
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Device Summary
Frequently Asked Questions
What is the TREATMENT TABLES, MANUALLY ACTIVATED?
TREATMENT TABLES, MANUALLY ACTIVATED is a medical device that received FDA 510(k) clearance on 1993-07-21. The listed applicant is Med Mart, Inc.. The 510(k) number is K931635.
When did TREATMENT TABLES, MANUALLY ACTIVATED receive FDA 510(k) clearance?
TREATMENT TABLES, MANUALLY ACTIVATED received FDA 510(k) clearance on 1993-07-21, under 510(k) number K931635.
Who is the listed applicant for TREATMENT TABLES, MANUALLY ACTIVATED?
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 TREATMENT TABLES, MANUALLY ACTIVATED?
The FDA product code for TREATMENT TABLES, MANUALLY ACTIVATED is INW.
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: INW)
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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