510(k) K883059
K883059 is an FDA 510(k) premarket notification submitted by Wako Chemicals USA, Inc. for the device "WAKO(TM) AUTOKIT AMYLASE". The FDA issued a decision of Substantially Equivalent on August 30, 1988. The device falls under product code CJA (Amyloclastic, Amylase), a Class II device regulated under 21 CFR 862.1070. Wako Chemicals USA, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 30, 1988
- Date Received
- July 19, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Amyloclastic, Amylase
- Device Class
- Class II
- Regulation Number
- 862.1070
- Review Panel
- CH
- Submission Type