CONNECTORS
FDA 510(k) clearance K760382 · decided 1976-11-02
Clearance details
- K-number
- K760382
- Device name
- CONNECTORS
- Applicant
- B. Braun Instruments
- Decision
- Substantially Equivalent
- Date received
- 1976-08-05
- Decision date
- 1976-11-02
- Days to decision
- 89 days
- Clearance type
- Traditional
- Product code
- GCD
- Device class
- 1
- Regulation number
- 878.4200
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- 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 |
|---|---|---|
| ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II. (K952470) | R-Group Intl. | 1995-11-28 |
| L-CATH CONNECTOR ASSEMBLY (K940198) | Luther Medical Products, Inc. | 1994-12-15 |
| ANGIOMED HIGH PRESSURE CONNECTORS (K863446) | Angiomed U.S., Inc. | 1986-09-23 |
| INCISION DRAIN (K851196) | Sil-Med Corp. | 1985-06-04 |
| Y CONNECTOR (K851921) | Sil-Med Corp. | 1985-05-17 |
| CATHETER CONNECTOR, ARGYLE TUBING (K760524) | Sherwood Medical Industries | 1976-11-02 |
| TUBE, STERILE NON-CONDUCTIVE CONNECTING (K760203) | Ipco Corp. | 1976-07-19 |
Recalls involving this device
No recalls on record reference this clearance.