TECHTON PROTECTIVE PAD
FDA 510(k) clearance K873038 · decided 1989-04-03
Clearance details
- K-number
- K873038
- Device name
- TECHTON PROTECTIVE PAD
- Applicant
- Techton, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-08-04
- Decision date
- 1989-04-03
- Days to decision
- 608 days
- Clearance type
- Traditional
- Product code
- IWQ
- Device class
- 1
- Regulation number
- 892.6500
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Albuquerque, NM, 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 |
|---|---|---|
| MAVIG LOWER BODY PROTECTION SYSTEMS, ASSEMBLY MODELS 6265, 6266, 6267, 6268, 6269/0, 629/1, AND 6269/2 (K945238) | F. Walter Hanel GmbH | 1994-12-15 |
| X-RAY DRAPES (K923099) | Hydro-Med Products, Inc. | 1992-10-15 |
Recalls involving this device
No recalls on record reference this clearance.