510(k) K860659
K860659 is an FDA 510(k) premarket notification submitted by Life Design Systems, Inc. for the device "END TIDAL CO2 SAMPLING CIRCUIT". The FDA issued a decision of Substantially Equivalent on April 17, 1986. The device falls under product code BZO (Set, Tubing And Support, Ventilator (W Harness)), a Class I device regulated under 21 CFR 868.5975. Life Design Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 17, 1986
- Date Received
- February 24, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Set, Tubing And Support, Ventilator (W Harness)
- Device Class
- Class I
- Regulation Number
- 868.5975
- Review Panel
- AN
- Submission Type