K924957Substantially Equivalent
Opus(r) Vancomycin
Pb Diagnostic Systems, Inc., Westwood MA / Traditional, Substantially Equivalent
K924957 is the FDA 510(k) clearance record for OPUS(R) VANCOMYCIN, a class II device, cleared for Pb Diagnostic Systems, Inc. on under FDA product code LEH (Radioimmunoassay, Vancomycin). FDA records list 35 510(k) clearances for Pb Diagnostic Systems, Inc., from to . As of , FDA records show no recalls naming K924957.
Clearance record
- Decision date
- Received
- (72 days to decision)
- Product code
- LEH Radioimmunoassay, Vancomycin
- Regulation
- 21 CFR 862.3950
- Device class
- Class II
- Review panel
- Clinical Toxicology
- Applicant
- Pb Diagnostic Systems, Inc. 151 University Ave., Westwood MA
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code LEH
Trailing 12 monthsFDA records hold no clearances under product code LEH 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.
