510(k) K902758
K902758 is an FDA 510(k) premarket notification submitted by Cobe Laboratories, Inc. for the device "COBE SATURATION/HEMATOCRIT MONITOR W/ FIBER OPTIC". The FDA issued a decision of Substantially Equivalent on August 23, 1990. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Cobe Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 23, 1990
- Date Received
- June 25, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Oximeter
- Device Class
- Class II
- Regulation Number
- 870.2700
- Review Panel
- AN
- Submission Type