510(k) K900755
K900755 is an FDA 510(k) premarket notification submitted by International Medical Products, Inc. for the device "DIGITAL CUFF PV GAUGE". The FDA issued a decision of Substantially Equivalent on April 26, 1990. The device falls under product code BSK (Cuff, Tracheal Tube, Inflatable), a Class II device regulated under 21 CFR 868.5750. International Medical Products, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 26, 1990
- Date Received
- February 16, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cuff, Tracheal Tube, Inflatable
- Device Class
- Class II
- Regulation Number
- 868.5750
- Review Panel
- AN
- Submission Type