LACERATION TRAY
K-Number: K932036 · 1993-12-13
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Device Summary
Frequently Asked Questions
What is the LACERATION TRAY?
LACERATION TRAY is a medical device that received FDA 510(k) clearance on 1993-12-13. The listed applicant is Clinipad Corp.. The 510(k) number is K932036.
When did LACERATION TRAY receive FDA 510(k) clearance?
LACERATION TRAY received FDA 510(k) clearance on 1993-12-13, under 510(k) number K932036.
Who is the listed applicant for LACERATION TRAY?
The FDA 510(k) record lists Clinipad Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LACERATION TRAY?
The FDA product code for LACERATION TRAY is FRG.
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 Clinipad Corp. 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: FRG)
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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