510(k) K803207
K803207 is an FDA 510(k) premarket notification submitted by Timeter Instrument Corp. for the device "REGULATOR, OXYGEN MECHANICAL". The FDA issued a decision of Substantially Equivalent on January 15, 1981. The device falls under product code CAN (Regulator, Pressure, Gas Cylinder), a Class I device regulated under 21 CFR 868.2700. Timeter Instrument Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 15, 1981
- Date Received
- December 18, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Regulator, Pressure, Gas Cylinder
- Device Class
- Class I
- Regulation Number
- 868.2700
- Review Panel
- AN
- Submission Type