K790682 is the FDA 510(k) clearance record for TONOTEST BLOOD PRESSURE DEVICE, cleared for Robert Bosch Corp. on . FDA records list 21 510(k) clearances for Robert Bosch Corp., from to . As of , FDA records show no recalls naming K790682.
Clearance record
- Decision date
- Received
- (0 days to decision)
- Review panel
- Unknown
- Applicant
- Robert Bosch Corp. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
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