A CALIPER
FDA 510(k) clearance K820659 · decided 1982-03-19
Clearance details
- K-number
- K820659
- Device name
- A CALIPER
- Applicant
- Twin City Surgical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-03-10
- Decision date
- 1982-03-19
- Days to decision
- 9 days
- Clearance type
- Traditional
- Product code
- KTZ
- Device class
- 1
- Regulation number
- 888.4150
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Twin City Surgical
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 |
|---|---|---|
| NK MEDICAL MICROMETER, MODEL MC001 (K921266) | Nk Biotechnical Engineering Co. | 1992-07-14 |
| SKYNDEX ELECTRONIC BODY FAT CALCULA (K841687) | Caldwell, Justiss & Co., Inc. | 1984-06-28 |
| SCOLIMETER (K831898) | Dr. Micheal A. Sabia | 1983-07-19 |
| ISOROBIC SKINFOLD CALIPER (K810116) | Fitness Motivation Institute of America | 1981-02-04 |
| PARKE-DAVIS TOTAL KNEE PROSTHESIS (K800363) | Warner-Lambert Co. | 1980-03-10 |
| TAPE MEASURE (K760521) | Mcgaw Laboratories | 1976-11-12 |
Recalls involving this device
No recalls on record reference this clearance.