K801246Substantially Equivalent
Oxford Human Milk Pasteuriser
Vickers America Medical Corp., Mchenry IL / Traditional, Substantially Equivalent
K801246 is the FDA 510(k) clearance record for OXFORD HUMAN MILK PASTEURISER, a class II device, cleared for Vickers America Medical Corp. on under FDA product code HGX (Pump, Breast, Powered). FDA records list 22 510(k) clearances for Vickers America Medical Corp., from to . As of , FDA records show no recalls naming K801246.
Clearance record
- Decision date
- Received
- (128 days to decision)
- Product code
- HGX Pump, Breast, Powered
- Regulation
- 21 CFR 884.5160
- Device class
- Class II
- Review panel
- Obstetrics/Gynecology
- Applicant
- Vickers America Medical Corp. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
Clearances, product code HGX
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 3 |
| January 2026 | 1 |
| February 2026 | 4 |
| March 2026 | 2 |
| April 2026 | 8 |
| May 2026 | 3 |
| June 2026 | 8 |
| July 2026 | 2 |
| August 2026 | 2 |
| September 2026 | 3 |
| 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.
