510(k) K930437
K930437 is an FDA 510(k) premarket notification submitted by Marco Ophthalmic, Inc. for the device "MARCO STANDARD RADIUSGAUGES". The FDA issued a decision of Substantially Equivalent on August 9, 1993. The device falls under product code HLF (Device, Measuring, Lens Radius, Ophthalmic), a Class I device regulated under 21 CFR 886.1430. Marco Ophthalmic, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 9, 1993
- Date Received
- January 26, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Measuring, Lens Radius, Ophthalmic
- Device Class
- Class I
- Regulation Number
- 886.1430
- Review Panel
- OP
- Submission Type