Gamma Phage Lysis Assay for the Identification of Bacillus Anthrac
K143592 is the FDA 510(k) clearance record for GAMMA PHAGE LYSIS ASSAY FOR THE IDENTIFICATION OF BACILLUS ANTHRAC, a class II device, cleared for The Surgeon General, Department of the Army on under FDA product code NVQ (Bacteriophage And Controls, B. Anthracis Lysis). FDA's definition for product code NVQ reads: "A gamma phage lysis assay intended for the identification of bacillus anthracis from non-hemolytic, aerobic gram positive colonies isolated from sheep blood agar. To aid in the laboratory identification of bacillus anthracis culture growth...". FDA records list 2 510(k) clearances for The Surgeon General, Department of the Army, from to . As of , FDA records show no recalls naming K143592.
Clearance record
- Decision date
- Received
- (119 days to decision)
- Product code
- NVQ Bacteriophage And Controls, B. Anthracis Lysis
- Regulation
- 21 CFR 866.3045
- Device class
- Class II
- Review panel
- Microbiology
- Applicant
- The Surgeon General, Department of the Army 1430 Veterans Dr., Fort Detrick MD
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code NVQ
Trailing 12 monthsFDA records hold no clearances under product code NVQ 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 |
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