ENDOTRACHEAL TUBE CHANGERS
FDA 510(k) clearance K102127 · decided 2010-08-27
Clearance details
- K-number
- K102127
- Device name
- ENDOTRACHEAL TUBE CHANGERS
- Applicant
- Instrumentation Industries, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2010-07-29
- Decision date
- 2010-08-27
- Days to decision
- 29 days
- Clearance type
- Special
- Product code
- LNZ
- Device class
- 2
- Regulation number
- 868.5730
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Bethel Park, PA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| ENDOTRACHEAL TUBE CHANGERS (P800068/S002) | Instrumentation Industries, Inc. | 1999-11-04 |
| ENDOTRACHEAL TUBE CHANGER (P800068/S001) | Instrumentation Industries, Inc. | 1999-07-23 |
| ENDOTRACHEAL TUBE CHANGER (P800068) | Instrumentation Industries, Inc. | 1981-07-21 |