PROD. NO. 02-031 - LACERATION TRAY
K-Number: K963443 · 1996-10-17
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Device Summary
Frequently Asked Questions
What is the PROD. NO. 02-031 - LACERATION TRAY?
PROD. NO. 02-031 - LACERATION TRAY is a medical device that received FDA 510(k) clearance on 1996-10-17. The listed applicant is Continental Medical Laboratories, Inc.. The 510(k) number is K963443.
When did PROD. NO. 02-031 - LACERATION TRAY receive FDA 510(k) clearance?
PROD. NO. 02-031 - LACERATION TRAY received FDA 510(k) clearance on 1996-10-17, under 510(k) number K963443.
Who is the listed applicant for PROD. NO. 02-031 - LACERATION TRAY?
The FDA 510(k) record lists Continental Medical Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROD. NO. 02-031 - LACERATION TRAY?
The FDA product code for PROD. NO. 02-031 - LACERATION 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 Continental Medical Laboratories, 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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