510(k) K974621
K974621 is an FDA 510(k) premarket notification submitted by E-Z-Em, Inc. for the device "PERCUPUMP II WITH EDA". The FDA issued a decision of Substantially Equivalent on January 27, 1998. The device falls under product code DSB (Plethysmograph, Impedance), a Class II device regulated under 21 CFR 870.2770. E-Z-Em, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 27, 1998
- Date Received
- December 11, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Plethysmograph, Impedance
- Device Class
- Class II
- Regulation Number
- 870.2770
- Review Panel
- CV
- Submission Type