510(k) K862812
K862812 is an FDA 510(k) premarket notification submitted by Nellcor, Inc. for the device "NELLCOR MVP, MODEL N-1000". The FDA issued a decision of Substantially Equivalent on December 22, 1986. The device falls under product code DQA (Oximeter), a Class II device regulated under 21 CFR 870.2700. Nellcor, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 22, 1986
- Date Received
- July 24, 1986
- 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