510(k) K830335
K830335 is an FDA 510(k) premarket notification submitted by Jedmed Instrument Co. for the device "DORC CORNEAL PUNCH BLOCK". The FDA issued a decision of Substantially Equivalent on March 9, 1983. The device falls under product code HNJ (Punch, Corneo-Scleral), a Class I device regulated under 21 CFR 886.4350. Jedmed Instrument Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 9, 1983
- Date Received
- February 1, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Punch, Corneo-Scleral
- Device Class
- Class I
- Regulation Number
- 886.4350
- Review Panel
- OP
- Submission Type