K023109Substantially Equivalent
Amedica Drug Screen Phencyclidine Test
Amedica Biotech, Inc., Hayward CA / Traditional, Substantially Equivalent
K023109 is the FDA 510(k) clearance record for AMEDICA DRUG SCREEN PHENCYCLIDINE TEST, cleared for Amedica Biotech, Inc. on under FDA product code LCM (Enzyme Immunoassay, Phencyclidine). FDA records list 13 510(k) clearances for Amedica Biotech, Inc., from to . As of , FDA records show no recalls naming K023109.
Clearance record
- Decision date
- Received
- (89 days to decision)
- Product code
- LCM Enzyme Immunoassay, Phencyclidine
- Device class
- Unclassified
- Review panel
- Unknown
- Applicant
- Amedica Biotech, Inc. 28301 Industrial Blvd. Suite K, Hayward CA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code LCM
Trailing 12 monthsFDA records hold no clearances under product code LCM 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.
