510(k) K802229
K802229 is an FDA 510(k) premarket notification submitted by Kem Medical Products Corp. for the device "CHEMICAL INDICATOR - KEM MED & BIO SURE". The FDA issued a decision of Substantially Equivalent on Dec 9, 1980. The device falls under product code JOJ (Indicator, Physical/Chemical Sterilization Process), a Class II device regulated under 21 CFR 880.2800. Kem Medical Products Corp. has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 9, 1980
- Date Received
- Sep 10, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Indicator, Physical/Chemical Sterilization Process
- Device Class
- Class II
- Regulation Number
- 880.2800
- Review Panel
- HO
- Submission Type
- 510(k)