510(k) K855050
K855050 is an FDA 510(k) premarket notification submitted by Storz Instrument Co. for the device "STORZ E9040 & E9046 DIAMOND KNIVES". The FDA issued a decision of Substantially Equivalent on March 5, 1986. The device falls under product code HNN (Knife, Ophthalmic), a Class I device regulated under 21 CFR 886.4350. Storz Instrument Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 5, 1986
- Date Received
- December 17, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Knife, Ophthalmic
- Device Class
- Class I
- Regulation Number
- 886.4350
- Review Panel
- OP
- Submission Type