LACERATTION TRAY
K-Number: K920763 · 1992-09-28
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Device Summary
Frequently Asked Questions
What is the LACERATTION TRAY?
LACERATTION TRAY is a medical device that received FDA 510(k) clearance on 1992-09-28. The listed applicant is Sterile Concepts, Inc.. The 510(k) number is K920763.
When did LACERATTION TRAY receive FDA 510(k) clearance?
LACERATTION TRAY received FDA 510(k) clearance on 1992-09-28, under 510(k) number K920763.
Who is the listed applicant for LACERATTION TRAY?
The FDA 510(k) record lists Sterile Concepts, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LACERATTION TRAY?
The FDA product code for LACERATTION TRAY is KDD.
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 Sterile Concepts, 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: KDD)
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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