E600B FOOTSWITCH
FDA 510(k) clearance K874794 · decided 1987-12-14
Clearance details
- K-number
- K874794
- Device name
- E600B FOOTSWITCH
- Applicant
- Valleylab, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-11-23
- Decision date
- 1987-12-14
- Days to decision
- 21 days
- Clearance type
- Traditional
- Product code
- BWA
- Device class
- 2
- Regulation number
- 878.4400
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Boulder, CO, 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 |
|---|---|---|
| ALEXANDER BOX, BATTERY, RECHARGEABLE (K963305) | Alexander Mfg. Co. | 1997-04-17 |
| EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001 (K873809) | Zimmer Aspen Labs | 1987-11-20 |
Recalls involving this device
No recalls on record reference this clearance.