VACVENT
FDA 510(k) clearance K931873 · decided 1993-12-30
Clearance details
- K-number
- K931873
- Device name
- VACVENT
- Applicant
- Steven Frank Mercereau
- Decision
- Unknown
- Date received
- 1993-04-14
- Decision date
- 1993-12-30
- Days to decision
- 260 days
- Clearance type
- Traditional
- Product code
- CBT
- Device class
- 1
- Regulation number
- 868.1100
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Conyers, GA, US
- Third-party review
- No
- Expedited review
- No
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|---|---|---|
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| ABC IN-LINE BLOOD SAMPLING KIT (K955663) | Utah Medical Products, Inc. | 1997-03-17 |
| ABG POINT LOK NEEDLE PROTECTION DEVICE (K954015) | Devon Industries, Inc. | 1995-11-20 |
| ACTI-FLEX ARTERIAL EXTENSION SET (K954035) | R-Group Intl. | 1995-09-25 |
| NEEDLE SAFETY COVER (K950098) | Hammer-Plane, Inc. | 1995-08-11 |
| ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM (K945719) | Sherwood Medical Co. | 1995-03-16 |
| PISTON SYRINGE (K944941) | Martell Medical Products, Inc. | 1994-12-05 |
| ABG NEEDLE PROTECTION (K945485) | Devon Industries, Inc. | 1994-11-29 |
| ASPIR-PULSE(TM) SAF-T-VENT (K940575) | Sherwood Medical Co. | 1994-03-22 |
| BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560 (K930986) | Customed, Inc. | 1993-07-14 |
| SHERWOOD MEDICAL ARTERIAL BLOOD GAS KIT I (K925453) | Sherwood Medical Co. | 1993-07-12 |
Recalls involving this device
No recalls on record reference this clearance.