K830947Substantially Equivalent
Syringe/needle Dispos-Box-Cutter/crimper
Post Medical, Inc., Mchenry IL / Traditional, Substantially Equivalent
K830947 is the FDA 510(k) clearance record for SYRINGE/NEEDLE DISPOS-BOX-CUTTER/CRIMPER, cleared for Post Medical, Inc. on . FDA records list 6 510(k) clearances for Post Medical, Inc., from to . As of , FDA records show no recalls naming K830947.
Clearance record
- Decision date
- Received
- (19 days to decision)
- Review panel
- Unknown
- Applicant
- Post Medical, Inc. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
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