MOLECTRON MEDICAL ND:YAG LASER, MODEL 8000
K-Number: K833480 · 1983-12-21
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Device Summary
Frequently Asked Questions
What is the MOLECTRON MEDICAL ND:YAG LASER, MODEL 8000?
MOLECTRON MEDICAL ND:YAG LASER, MODEL 8000 is a medical device that received FDA 510(k) clearance on 1983-12-21. The listed applicant is Cooper Lasersonics, Inc.. The 510(k) number is K833480.
When did MOLECTRON MEDICAL ND:YAG LASER, MODEL 8000 receive FDA 510(k) clearance?
MOLECTRON MEDICAL ND:YAG LASER, MODEL 8000 received FDA 510(k) clearance on 1983-12-21, under 510(k) number K833480.
Who is the listed applicant for MOLECTRON MEDICAL ND:YAG LASER, MODEL 8000?
The FDA 510(k) record lists Cooper Lasersonics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOLECTRON MEDICAL ND:YAG LASER, MODEL 8000?
The FDA product code for MOLECTRON MEDICAL ND:YAG LASER, MODEL 8000 is LNK.
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 Cooper Lasersonics, 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: LNK)
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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