BE #16 - MANIFOLD
FDA 510(k) clearance K823481 · decided 1982-12-22
Clearance details
- K-number
- K823481
- Device name
- BE #16 - MANIFOLD
- Applicant
- Instrumentation Industries, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-11-23
- Decision date
- 1982-12-22
- Days to decision
- 29 days
- Clearance type
- Traditional
- Product code
- BZO
- Device class
- 1
- Regulation number
- 868.5975
- 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 |
|---|---|---|
| UNICOR, INC. CORRUGATED TUBING (K953784) | Unicor, Inc. | 1995-09-19 |
| UNICOR, INC. VENTILATOR HOSES (K953785) | Unicor, Inc. | 1995-09-18 |
| PRIMA VENTILATOR HOSES (K952010) | Prima, Inc. | 1995-05-22 |
| PRIMA VOLUMN VENTILATORSS (K952022) | Prima, Inc. | 1995-05-22 |
| PRIMA CUSTOM ANESTESIA CIRCUIT (K952012) | Prima, Inc. | 1995-05-22 |
| PRIMA BREATHING BAGS (K952011) | Prima, Inc. | 1995-05-22 |
| INFANT FLOW SYSTEM (K945740) | Hamilton Medical, Inc. | 1995-03-23 |
| PRIMA, INC. CORRUGATED TUBING (K944531) | Prima, Inc. | 1994-12-02 |
| VENTILATOR HOSE (K942569) | Med-Plastics Intl., Inc. | 1994-06-10 |
| VOLUME VENTILATOR (K942572) | Med-Plastics Intl., Inc. | 1994-06-10 |
| TUBE, INHALER OXYGEN (K935582) | Puritas Health Care, Inc. | 1994-01-14 |
| STAR BREATHING CIRCUITS (K934753) | Infrasonics Corp. | 1993-10-27 |
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 |