IMPULS 3, IT SELECTOR
FDA 510(k) clearance K842805 · decided 1984-08-01
Clearance details
- K-number
- K842805
- Device name
- IMPULS 3, IT SELECTOR
- Applicant
- Robert Bosch Corp.
- Decision
- Substantially Equivalent
- Date received
- 1984-07-17
- Decision date
- 1984-08-01
- Days to decision
- 15 days
- Clearance type
- Traditional
- Product code
- ISB
- Device class
- 2
- Regulation number
- 890.1850
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Robert Bosch Corp.
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| PIRD-Y (K842262) | Pirdy, Inc. | 1984-06-28 |
| GALVANIC UNIT (K790949) | Rami International Corp. | 1979-08-16 |
| MAXICEPTOR (K780632) | Med General | 1978-08-14 |
| FIGURETRIM (K780730) | Jay-Mar INternational Enterprises, IN | 1978-05-09 |
Recalls involving this device
No recalls on record reference this clearance.