MULTICAM I 8X10
K-Number: K912341 · 1991-08-26
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Device Summary
Frequently Asked Questions
What is the MULTICAM I 8X10?
MULTICAM I 8X10 is a medical device that received FDA 510(k) clearance on 1991-08-26. The listed applicant is Camtronics, Ltd.. The 510(k) number is K912341.
When did MULTICAM I 8X10 receive FDA 510(k) clearance?
MULTICAM I 8X10 received FDA 510(k) clearance on 1991-08-26, under 510(k) number K912341.
Who is the listed applicant for MULTICAM I 8X10?
The FDA 510(k) record lists Camtronics, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTICAM I 8X10?
The FDA product code for MULTICAM I 8X10 is JAA.
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 Camtronics, Ltd. 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: JAA)
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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