510(k) K851888
K851888 is an FDA 510(k) premarket notification submitted by Honeywell, Inc. for the device "APM DISPOS. BLOOD PRESSURE TRANSDUCER". The FDA issued a decision of Substantially Equivalent on August 6, 1985. The device falls under product code DRS (Transducer, Blood-Pressure, Extravascular), a Class II device regulated under 21 CFR 870.2850. Honeywell, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 6, 1985
- Date Received
- May 1, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Transducer, Blood-Pressure, Extravascular
- Device Class
- Class II
- Regulation Number
- 870.2850
- Review Panel
- CV
- Submission Type