510(k) K973970
K973970 is an FDA 510(k) premarket notification submitted by Medical Cables, Inc. for the device "SPO2 FINGER PROBES". The FDA issued a decision of Substantially Equivalent on October 6, 1998. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Medical Cables, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 6, 1998
- Date Received
- October 17, 1997
- 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