STERILE LACERATION & DEBRIDEMENT TRAYS
K-Number: K934029 · 1994-02-04
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Device Summary
Frequently Asked Questions
What is the STERILE LACERATION & DEBRIDEMENT TRAYS?
STERILE LACERATION & DEBRIDEMENT TRAYS is a medical device that received FDA 510(k) clearance on 1994-02-04. The listed applicant is Surgipro, Inc.. The 510(k) number is K934029.
When did STERILE LACERATION & DEBRIDEMENT TRAYS receive FDA 510(k) clearance?
STERILE LACERATION & DEBRIDEMENT TRAYS received FDA 510(k) clearance on 1994-02-04, under 510(k) number K934029.
Who is the listed applicant for STERILE LACERATION & DEBRIDEMENT TRAYS?
The FDA 510(k) record lists Surgipro, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE LACERATION & DEBRIDEMENT TRAYS?
The FDA product code for STERILE LACERATION & DEBRIDEMENT TRAYS 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 Surgipro, 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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