FOREARM-CANE
FDA 510(k) clearance K790299 · decided 1979-02-21
Clearance details
- K-number
- K790299
- Device name
- FOREARM-CANE
- Applicant
- Guardian Products Co., Inc.
- Decision
- Substantially Equivalent
- Date received
- 1979-02-12
- Decision date
- 1979-02-21
- Days to decision
- 9 days
- Clearance type
- Traditional
- Product code
- IPS
- Device class
- 1
- Regulation number
- 890.3075
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- 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 |
|---|---|---|
| CANE REACHER (K832970) | Maddak, Inc. | 1983-09-29 |
| WALKING CANE (K832969) | Maddak, Inc. | 1983-09-29 |
| LIGHT WEIGHT ALUMINUM CANES (K821402) | Manuco Manufacturing Co., Inc. | 1982-04-21 |
| CERSA-CANE (K790558) | Maddak, Inc. | 1979-04-03 |
| OFFSET ALUMINUM CANE (K790561) | Maddak, Inc. | 1979-04-03 |
| CANE/REACHER (K780085) | Fred Sammons, Inc. | 1978-01-30 |
| QUADRAPLEGIC WALKING AID (K772267) | Med Fusion Systems, Inc. | 1977-12-20 |
| UNICET I (K770529) | Union Carbide Corp. | 1977-04-05 |
Recalls involving this device
No recalls on record reference this clearance.