K052649Substantially Equivalent
Drg Slv Testosterone Elisa Test
Drg Intl., Inc., East Stroudsburg PA / Traditional, Substantially Equivalent
K052649 is the FDA 510(k) clearance record for DRG SLV TESTOSTERONE ELISA TEST, a class I device, cleared for Drg Intl., Inc. on under FDA product code CDZ (Radioimmunoassay, Testosterones And Dihydrotestosterone). FDA records list 4 510(k) clearances for Drg Intl., Inc., from to . As of , FDA records show 2 recalls naming K052649.
Clearance record
- Decision date
- Received
- (123 days to decision)
- Product code
- CDZ Radioimmunoassay, Testosterones And Dihydrotestosterone
- Regulation
- 21 CFR 862.1680
- Device class
- Class I
- Review panel
- Clinical Chemistry
- Applicant
- Drg Intl., Inc. 150 Cherry Ln. Rd., East Stroudsburg PA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code CDZ
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 1 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
