510(k) K960194
K960194 is an FDA 510(k) premarket notification submitted by Myelotec, Inc. for the device "MYELOTEC MYELOSCOPE". The FDA issued a decision of Substantially Equivalent on September 4, 1996. The device falls under product code HRX (Arthroscope), a Class II device regulated under 21 CFR 888.1100. Myelotec, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 4, 1996
- Date Received
- January 16, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Arthroscope
- Device Class
- Class II
- Regulation Number
- 888.1100
- Review Panel
- OR
- Submission Type
Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).