510(k) K864200
- Device
- Veta/vented Esophageal Tube Airway
- Applicant
- CRANCO CO.
- 510(k) number
- K864200
- Product code
- CAO
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1987-03-17
- Date received
- 1986-10-27
- Regulation
- 868.5650
- Classification name
- Airway, Esophageal (Obturator)
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- RICHARD CRANGLE
- Address
- 120 Oakwood Plz. 5320 S. 900 E. Salt Lake City UT US 84117 84117
FDA Registration Numbers#
- 9681384
- 3020460367
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code CAO#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K971348 | FASTTRACH SINGLE-PASS TRACHEAL/ESOPHAGEAL AIRWAY SYSTEM | Green Field Medical Sourcing, Inc. | 1998-02-27 |
| K894032 | EVAC-TUBE | Sharn, Inc. | 1989-08-31 |
| K875226 | ESOPHAGEAL OBTURATOR/TRACHEAL TUBE | Sheridan Catheter Corp. | 1988-01-19 |
| K863172 | RESPIRONICS PTL REVIVEEASY | Respironics, Inc. | 1986-11-04 |
| K761195 | ESOPHAGEAL OBTURATION AIRWAY | Mckesson Corp. | 1976-12-09 |