Micrusframe (Mfr100202); Micrusframe (Mfr100253); Micrusframe (Mfr100305); Micrusframe (Mfr100356); Micrusframe (Mfr100407); Micrusframe (Mfr100412); Micrusframe (Mfr100509); Micrusframe (Mfr100517); Micrusframe (Mfr100611); Micrusframe (Mfr100626); Micrusframe (Mfr100713); Micrusframe (Mfr100730); Micrusframe (Mfr100816); Micrusframe (Mfr100829); Micrusframe (Mfr140225); Micrusframe (Mfr140303); Micrusframe (Mfr140304); Micrusframe (Mfr140306); Micrusframe (Mfr140406); Micrusframe (Mf
K262419 is the FDA 510(k) clearance record for MICRUSFRAME (MFR100202); MICRUSFRAME (MFR100253); MICRUSFRAME (MFR100305); MICRUSFRAME (MFR100356); MICRUSFRAME (MFR100407); MICRUSFRAME (MFR100412); MICRUSFRAME (MFR100509); MICRUSFRAME (MFR100517); MICRUSFRAME (MFR100611); MICRUSFRAME (MFR100626); MICRUSFRAME (MFR100713); MICRUSFRAME (MFR100730); MICRUSFRAME (MFR100816); MICRUSFRAME (MFR100829); MICRUSFRAME (MFR140225); MICRUSFRAME (MFR140303); MICRUSFRAME (MFR140304); MICRUSFRAME (MFR140306); MICRUSFRAME (MFR140406); MICRUSFRAME (MF, a class II device, cleared for Cerenovus, Inc. on under FDA product code HCG (Device, Neurovascular Embolization). FDA records list 163 510(k) clearances for Cerenovus, Inc., from to . As of , FDA records show no recalls naming K262419.
Clearance record
- Decision date
- Received
- (30 days to decision)
- Product code
- HCG Device, Neurovascular Embolization
- Regulation
- 21 CFR 882.5950
- Device class
- Class II
- Review panel
- Neurology
- Applicant
- Cerenovus, Inc. 31 Technology Dr., Irvine CA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code HCG
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 1 |
| January 2026 | 1 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 1 |
| June 2026 | 1 |
| July 2026 | 0 |
| August 2026 | 1 |
| September 2026 | 0 |
| October 2026 | 0 |
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