510(k) K853180
K853180 is an FDA 510(k) premarket notification submitted by Keeler Instruments, Inc. for the device "VICKERS ERGOMATIC MICROS INSTR-LONG R OR L HANDED". The FDA issued a decision of Substantially Equivalent on October 28, 1985. The device falls under product code GZX (Instrument, Microsurgical), a Class I device regulated under 21 CFR 882.4525. Keeler Instruments, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 28, 1985
- Date Received
- July 30, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Instrument, Microsurgical
- Device Class
- Class I
- Regulation Number
- 882.4525
- Review Panel
- NE
- Submission Type