Conphar Crutch Grips
FDA 510(k) K803140 · Conphar, Inc.
510(k) numberK803140
Submission
- Device name
- Conphar Crutch Grips
- Applicant
- Conphar, Inc.
Mchenry, IL, US - Received
- December 12, 1980
- Decision date
- January 8, 1981
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- INP – Tips And Pads, Cane, Crutch And Walker
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 890.3790
- Specialty
- Physical Medicine
Other 510(k)s with product code INP
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K831889 | Surgeon's Choice Crutch HandleINP · Traditional | W.K. Wheeler, Inc. | 07/07/1983SE |
| K831149 | Personal Knee Crutch PadINP · Traditional | Tecnol New Jersey Wound Care, Inc. | 05/03/1983SE |
| K811493 | Crutch & Walker PadsINP · Traditional | Fred Sammons, Inc. | 06/12/1981SE |
| K810650 | Crutch Tips & GripsINP · Traditional | First Industries, Inc. | 03/26/1981SE |
| K803144 | Conphar Crutch PadsINP · Traditional | Conphar, Inc. | 01/08/1981SE |
| K803136 | Conphar Crutch TipsINP · Traditional | Conphar, Inc. | 01/08/1981SE |
| K800076 | Crutch Tips, Pads & Hand GripsINP · Traditional | New World Imports, Inc. | 01/28/1980SE |
More from New World Imports, Inc.
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|---|---|---|
| K821825 | Conphar Silicone Feeding TubeKNT · Traditional | 08/10/1982SE |
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| K821295 | Olsen Hegar Needle HoldersGDF · Traditional | 06/03/1982SE |
| K821289 | Mayo-Hegar Needle HolderGDF · Traditional | 06/03/1982SE |
| K821298 | Backhaus Clamp, 3 1/2HTD · Traditional | 05/28/1982SE |
| K821294 | Tonsil Scissors Straight 5 1/2EGN · Traditional | 05/28/1982SE |
| K821293 | Backhaus Clamp, 5 1/4HTD · Traditional | 05/28/1982SE |
| K821292 | Tonsil Scissors 7EGN · Traditional | 05/28/1982SE |
| K821290 | Littauer Scissors 5 1/2HNF · Traditional | 05/28/1982SE |
| K821286 | Iris Scissors Straight 4 1/2HNF · Traditional | 05/28/1982SE |
Questions and answers
When was Conphar Crutch Grips cleared by the FDA?
Conphar Crutch Grips (K803140) received a 510(k) decision of Substantially Equivalent on January 8, 1981, 27 days after the submission was received.
What is the product code of K803140?
The FDA product code is INP – Tips And Pads, Cane, Crutch And Walker, a Class I (low risk) device regulated under 21 CFR 890.3790.