510(k) K911124
K911124 is an FDA 510(k) premarket notification submitted by Criticare Systems, Inc. for the device "503 PULSE OXIMETER". The FDA issued a decision of Substantially Equivalent on Jun 7, 1991. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Criticare Systems, Inc. has 21 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 7, 1991
- Date Received
- Mar 12, 1991
- 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
- 510(k)