VISION-STIMULATOR, CAM
K-Number: K781313 · 1979-01-26
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Device Summary
Frequently Asked Questions
What is the VISION-STIMULATOR, CAM?
VISION-STIMULATOR, CAM is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is Clement Clarke, Inc.. The 510(k) number is K781313.
When did VISION-STIMULATOR, CAM receive FDA 510(k) clearance?
VISION-STIMULATOR, CAM received FDA 510(k) clearance on 1979-01-26, under 510(k) number K781313.
Who is the listed applicant for VISION-STIMULATOR, CAM?
The FDA 510(k) record lists Clement Clarke, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VISION-STIMULATOR, CAM?
The FDA product code for VISION-STIMULATOR, CAM is HPL.
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 Clement Clarke, 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: HPL)
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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