A.V.R. KNEE LENGTH THERAPEUTIC STOCK-
FDA 510(k) clearance K832609 · decided 1983-09-12
Clearance details
- K-number
- K832609
- Device name
- A.V.R. KNEE LENGTH THERAPEUTIC STOCK-
- Applicant
- The Kendal Co.
- Decision
- Substantially Equivalent
- Date received
- 1983-08-03
- Decision date
- 1983-09-12
- Days to decision
- 40 days
- Clearance type
- Traditional
- Product code
- DWL
- Device class
- 2
- Regulation number
- 880.5780
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Walker, MI, 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 |
|---|
| MEDLINE ANTI-EMBOLISM STOCKING (K141127) | Medline Industries, Inc. | 2014-08-21 |
| BELLAVAR / CUSTOM SEAMLESS SOFT (A.K.A. COMTESSE) (K131496) | Bsn Medical, Inc. | 2013-07-10 |
| ENCIRCLE COMPRESSION THERAPY STOCKING (K122485) | Encircle Medical Devices , Ltd. | 2013-04-23 |
| BOSSONG HOSIERY MEDICAL COMPRESSION STOCKINGS 8-15 MMHG, BOSSONG HOSIERY ANTI-EMBOLISM STOCKINGS 10-20 MMHG, BOSSONG HOS (K123820) | Bossong Hosiery Mills, Inc. | 2013-04-02 |
| FUTURO (TM) TRAVEL KNEE-HIGHS; FUTURO (TM) TRAVEL SOCKS; FUTURO (TM) TRAVEL STOCKINGS; FUTURO (TM) TRAVEL PANTYHOSE (K123085) | 3M Company | 2012-12-20 |
| ELVAREX/ELVAREX SOFT/ELVAREX SOFT SEAMLESS (K123561) | Bsn Medical, Inc. | 2012-12-18 |
| DR. SCHOLL'S COMPRESSION SOCKS (K123398) | Renfro Corporation | 2012-12-18 |
| TRUFORM READY-TO-WEAR COMPRESSION ARM SLEECE TRUFORM READY-TO-WEAR COMPRESSION GAUNTLET (K121106) | Surgical Appliance Industries, Inc. | 2012-04-27 |
| CURAD COMPRESSION HOSIERY (K112769) | Medline Industries, Inc. | 2012-03-01 |
| VENOTRAIN CURAFLOW (K111662) | Bauerfeind AG | 2011-10-04 |
| HEELSAFE DVT HOSE, MODELS 00800-00804, 00805-00809 (K101614) | Dm Systems, Incorporated | 2011-01-13 |
| SAPHENAMEDICAL ANTI-EMBOLISM STOCKINGS (K101224) | Griffiths and Nielsen, Ltd. | 2010-12-03 |
Recalls involving this device
No recalls on record reference this clearance.