K772228Substantially Equivalent
Alsite Magnivision
Al Nyman & Son, Inc., Mchenry IL / Traditional, Substantially Equivalent
K772228 is the FDA 510(k) clearance record for ALSITE MAGNIVISION, cleared for Al Nyman & Son, Inc. on . FDA records list one 510(k) clearance for Al Nyman & Son, Inc. As of , FDA records show no recalls naming K772228.
Clearance record
- Decision date
- Received
- (28 days to decision)
- Review panel
- Unknown
- Applicant
- Al Nyman & Son, Inc. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
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