POWER OPTIC
K-Number: K831976 · 1983-08-12
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Device Summary
Frequently Asked Questions
What is the POWER OPTIC?
POWER OPTIC is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Ritter Co.. The 510(k) number is K831976.
When did POWER OPTIC receive FDA 510(k) clearance?
POWER OPTIC received FDA 510(k) clearance on 1983-08-12, under 510(k) number K831976.
Who is the listed applicant for POWER OPTIC?
The FDA 510(k) record lists Ritter Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWER OPTIC?
The FDA product code for POWER OPTIC is EAY.
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 Ritter Co. 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: EAY)
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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