510(k) K984338
K984338 is an FDA 510(k) premarket notification submitted by Jostra Bentley for the device "JOSTRA HL-20 TWIN PUMP". The FDA issued a decision of Substantially Equivalent on August 19, 1999. The device falls under product code DPW (Flowmeter, Blood, Cardiovascular), a Class II device regulated under 21 CFR 870.2100. Jostra Bentley has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 19, 1999
- Date Received
- December 3, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Flowmeter, Blood, Cardiovascular
- Device Class
- Class II
- Regulation Number
- 870.2100
- Review Panel
- CV
- Submission Type