LASER RECTOSCOPE SET 784
K-Number: K842997 · 1984-08-27
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Device Summary
Frequently Asked Questions
What is the LASER RECTOSCOPE SET 784?
LASER RECTOSCOPE SET 784 is a medical device that received FDA 510(k) clearance on 1984-08-27. The listed applicant is Laser Industries , Ltd.. The 510(k) number is K842997.
When did LASER RECTOSCOPE SET 784 receive FDA 510(k) clearance?
LASER RECTOSCOPE SET 784 received FDA 510(k) clearance on 1984-08-27, under 510(k) number K842997.
Who is the listed applicant for LASER RECTOSCOPE SET 784?
The FDA 510(k) record lists Laser Industries , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LASER RECTOSCOPE SET 784?
The FDA product code for LASER RECTOSCOPE SET 784 is FDC.
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 Laser Industries , 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: FDC)
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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