MEDICAL PROCEDURE TRAY
K-Number: K902410 · 1990-11-20
Advertisement
Device Summary
Frequently Asked Questions
What is the MEDICAL PROCEDURE TRAY?
MEDICAL PROCEDURE TRAY is a medical device that received FDA 510(k) clearance on 1990-11-20. The listed applicant is Sorex Medical. The 510(k) number is K902410.
When did MEDICAL PROCEDURE TRAY receive FDA 510(k) clearance?
MEDICAL PROCEDURE TRAY received FDA 510(k) clearance on 1990-11-20, under 510(k) number K902410.
Who is the listed applicant for MEDICAL PROCEDURE TRAY?
The FDA 510(k) record lists Sorex Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDICAL PROCEDURE TRAY?
The FDA product code for MEDICAL PROCEDURE TRAY is LDQ.
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 Sorex Medical 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: LDQ)
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.
Advertisement