MEDSURG O.R. PROCEDURE TRAY
K-Number: K914037 · 1993-06-22
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Device Summary
Frequently Asked Questions
What is the MEDSURG O.R. PROCEDURE TRAY?
MEDSURG O.R. PROCEDURE TRAY is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K914037.
When did MEDSURG O.R. PROCEDURE TRAY receive FDA 510(k) clearance?
MEDSURG O.R. PROCEDURE TRAY received FDA 510(k) clearance on 1993-06-22, under 510(k) number K914037.
Who is the listed applicant for MEDSURG O.R. PROCEDURE TRAY?
The FDA 510(k) record lists Medsurg Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDSURG O.R. PROCEDURE TRAY?
The FDA product code for MEDSURG O.R. PROCEDURE TRAY is LRO.
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 Medsurg Industries, 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: LRO)
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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