510(k) K943234
K943234 is an FDA 510(k) premarket notification submitted by Marco Ophthalmic, Inc. for the device "MS-30 AUTOMATIC PERIMETER". The FDA issued a decision of Substantially Equivalent on July 27, 1994. The device falls under product code HPT (Perimeter, Automatic, Ac-Powered), a Class I device regulated under 21 CFR 886.1605. Marco Ophthalmic, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 27, 1994
- Date Received
- July 6, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Perimeter, Automatic, Ac-Powered
- Device Class
- Class I
- Regulation Number
- 886.1605
- Review Panel
- OP
- Submission Type