510(k) K821049
- Device
- PARATHERM
- Applicant
- American Thermometer Company, Inc.
- 510(k) number
- K821049
- Product code
- KYA
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1982-04-29
- Date received
- 1982-04-06
- Regulation
- 884.2982
- Classification name
- System, Thermographic, Liquid Crystal, Nonpowered (Adjunctive Use)
- Medical specialty
- Obstetrics/Gynecology
- Review panel
- Obstetrics/Gynecology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 2247290
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code KYA#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K900404 | VARICOSCREEN(TM) | Promedex, Inc. | 1990-12-07 |
| K832989 | BREAST THERMAL ACTIVITY INDICATOR | Bcsi Laboratories, Inc. | 1984-01-17 |
| K823245 | THERMAX; THERMAX SYSTEM | American Thermometer Company, Inc. | 1982-11-16 |
| K821524 | CHIROPRATIC INFRA-RED CRYSTAL PAK | Dr. John D. Reid B.A., D.C. | 1982-09-08 |