510(k) K834214
K834214 is an FDA 510(k) premarket notification submitted by Wescor, Inc. for the device "WESCOR 5500 VAPOR PRESSURE OSMOMETER". The FDA issued a decision of Substantially Equivalent on March 30, 1984. The device falls under product code JJM (Osmometer For Clinical Use), a Class I device regulated under 21 CFR 862.2730. Wescor, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 30, 1984
- Date Received
- December 5, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Osmometer For Clinical Use
- Device Class
- Class I
- Regulation Number
- 862.2730
- Review Panel
- CH
- Submission Type