K837046Substantially Equivalent
Autofocus Probe for Use with Ultrasound Autosector System
Technicare Corp., Solon OH / Traditional, Substantially Equivalent
K837046 is the FDA 510(k) clearance record for AUTOFOCUS PROBE FOR USE WITH ULTRASOUND AUTOSECTOR SYSTEM, cleared for Technicare Corp. on . FDA records list 32 510(k) clearances for Technicare Corp., from to . As of , FDA records show no recalls naming K837046.
Clearance record
- Decision date
- Received
- (81 days to decision)
- Review panel
- Unknown
- Applicant
- Technicare Corp. 29100 Aurora Rd., Solon OH
- Third party review
- No
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