483
Olympus Optical Co., Ltd.Olympus Optical Co., Ltd. – FDA 483
Record Details
This document is a 510(k) premarket notification summary and clearance letter for Olympus Optical Co., Ltd.'s Distal Attachment devices, not an FDA Form 483. As such, there are no inspectional observations or cited violations, indicating no severity issues from an inspectional standpoint.
- Company
- Olympus Optical Co., Ltd.
- Product type
- device
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ID · f90ea1aa-0fc6-4e25-90ad-d92f83f8c38a
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