ESOPHAGEAL OBTURATION AIRWAY
FDA 510(k) clearance K761195 · decided 1976-12-09
Clearance details
- K-number
- K761195
- Device name
- ESOPHAGEAL OBTURATION AIRWAY
- Applicant
- Mckesson Corp.
- Decision
- Substantially Equivalent
- Date received
- 1976-12-06
- Decision date
- 1976-12-09
- Days to decision
- 3 days
- Clearance type
- Traditional
- Product code
- CAO
- Device class
- 2
- Regulation number
- 868.5650
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| FASTTRACH SINGLE-PASS TRACHEAL/ESOPHAGEAL AIRWAY SYSTEM (K971348) | Green Field Medical Sourcing, Inc. | 1998-02-27 |
| EVAC-TUBE (K894032) | Sharn, Inc. | 1989-08-31 |
| ESOPHAGEAL OBTURATOR/TRACHEAL TUBE (K875226) | Sheridan Catheter Corp. | 1988-01-19 |
| VETA/VENTED ESOPHAGEAL TUBE AIRWAY (K864200) | Cranco Co. | 1987-03-17 |
| RESPIRONICS PTL REVIVEEASY (K863172) | Respironics, Inc. | 1986-11-04 |
Recalls involving this device
No recalls on record reference this clearance.