CARAPACE CATARACT TRAYS
K-Number: K931673 · 1993-12-30
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Device Summary
Frequently Asked Questions
What is the CARAPACE CATARACT TRAYS?
CARAPACE CATARACT TRAYS is a medical device that received FDA 510(k) clearance on 1993-12-30. The listed applicant is Carapace, Inc.. The 510(k) number is K931673.
When did CARAPACE CATARACT TRAYS receive FDA 510(k) clearance?
CARAPACE CATARACT TRAYS received FDA 510(k) clearance on 1993-12-30, under 510(k) number K931673.
Who is the listed applicant for CARAPACE CATARACT TRAYS?
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 CATARACT TRAYS?
The FDA product code for CARAPACE CATARACT 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 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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