510(k) K761195
- Device
- ESOPHAGEAL OBTURATION AIRWAY
- Applicant
- Mckesson Corp.
- 510(k) number
- K761195
- Product code
- CAO
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1976-12-09
- Date received
- 1976-12-06
- Regulation
- 868.5650
- Classification name
- Airway, Esophageal (Obturator)
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
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 |
| K864200 | VETA/VENTED ESOPHAGEAL TUBE AIRWAY | Cranco Co. | 1987-03-17 |
| K863172 | RESPIRONICS PTL REVIVEEASY | Respironics, Inc. | 1986-11-04 |