CARAPACE INSTRUMLENT AND INSTRUMENT SETS
K-Number: K931824 · 1993-12-06
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Device Summary
Frequently Asked Questions
What is the CARAPACE INSTRUMLENT AND INSTRUMENT SETS?
CARAPACE INSTRUMLENT AND INSTRUMENT SETS is a medical device that received FDA 510(k) clearance on 1993-12-06. The listed applicant is Carapace, Inc.. The 510(k) number is K931824.
When did CARAPACE INSTRUMLENT AND INSTRUMENT SETS receive FDA 510(k) clearance?
CARAPACE INSTRUMLENT AND INSTRUMENT SETS received FDA 510(k) clearance on 1993-12-06, under 510(k) number K931824.
Who is the listed applicant for CARAPACE INSTRUMLENT AND INSTRUMENT SETS?
The FDA 510(k) record lists Carapace, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARAPACE INSTRUMLENT AND INSTRUMENT SETS?
The FDA product code for CARAPACE INSTRUMLENT AND INSTRUMENT SETS 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 Carapace, 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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