510(k) K841369
K841369 is an FDA 510(k) premarket notification submitted by Orange Medical Instruments, Inc. for the device "BETA SCAN DRYSTIX". The FDA issued a decision of Substantially Equivalent on August 23, 1984. The device falls under product code CGA (Glucose Oxidase, Glucose), a Class II device regulated under 21 CFR 862.1345. Orange Medical Instruments, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 23, 1984
- Date Received
- April 3, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Glucose Oxidase, Glucose
- Device Class
- Class II
- Regulation Number
- 862.1345
- Review Panel
- CH
- Submission Type