510(k) K920337
K920337 is an FDA 510(k) premarket notification submitted by Heraeus Kulzer, Inc. for the device "MILES LIPASE SERA-PAK METHOD". The FDA issued a decision of Substantially Equivalent on March 11, 1992. The device falls under product code CHI (Lipase-Esterase, Enzymatic, Photometric, Lipase), a Class I device regulated under 21 CFR 862.1465. Heraeus Kulzer, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 11, 1992
- Date Received
- January 24, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lipase-Esterase, Enzymatic, Photometric, Lipase
- Device Class
- Class I
- Regulation Number
- 862.1465
- Review Panel
- CH
- Submission Type