K841086Substantially Equivalent
Surgical Instrument Demagnetizer
Scanlan Intl., Inc., Mchenry IL / Traditional, Substantially Equivalent
K841086 is the FDA 510(k) clearance record for SURGICAL INSTRUMENT DEMAGNETIZER, cleared for Scanlan Intl., Inc. on . FDA records list 19 510(k) clearances for Scanlan Intl., Inc., from to . As of , FDA records show no recalls naming K841086.
Clearance record
- Decision date
- Received
- (42 days to decision)
- Review panel
- Unknown
- Applicant
- Scanlan Intl., Inc. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
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.
