PATIENT PREOPERATIVE PREP TRAY, SINGLE USE
K-Number: K930270 · 1994-02-17
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Device Summary
Frequently Asked Questions
What is the PATIENT PREOPERATIVE PREP TRAY, SINGLE USE?
PATIENT PREOPERATIVE PREP TRAY, SINGLE USE is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Professional Medical Products, Inc.. The 510(k) number is K930270.
When did PATIENT PREOPERATIVE PREP TRAY, SINGLE USE receive FDA 510(k) clearance?
PATIENT PREOPERATIVE PREP TRAY, SINGLE USE received FDA 510(k) clearance on 1994-02-17, under 510(k) number K930270.
Who is the listed applicant for PATIENT PREOPERATIVE PREP TRAY, SINGLE USE?
The FDA 510(k) record lists Professional Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT PREOPERATIVE PREP TRAY, SINGLE USE?
The FDA product code for PATIENT PREOPERATIVE PREP TRAY, SINGLE USE 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 Professional Medical Products, 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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