Enzyme Immunoassay for the Detection of Salivary Cortisol
K051733 is the FDA 510(k) clearance record for ENZYME IMMUNOASSAY FOR THE DETECTION OF SALIVARY CORTISOL, a class II device, cleared for Drg Intl., Inc. on under FDA product code NHG (Enzyme Immunoassay, Cortisol, Salivary). FDA's definition for product code NHG reads: "The HS Salivary Cortisol Enzyme Immunoassay Kit is for the quantitative in vitro diagnostic measurement of salivary cortisol. This kit may be used to measure adrenal cortical function and as a screen for Cushing's and Addison's Disease...". FDA records list 4 510(k) clearances for Drg Intl., Inc., from to . As of , FDA records show no recalls naming K051733.
Clearance record
- Decision date
- Received
- (162 days to decision)
- Product code
- NHG Enzyme Immunoassay, Cortisol, Salivary
- Regulation
- 21 CFR 862.1205
- Device class
- Class II
- 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 NHG
Trailing 12 monthsFDA records hold no clearances under product code NHG in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| 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.
