510(k) K842005
K842005 is an FDA 510(k) premarket notification submitted by Camino Laboratories, Inc. for the device "MODEL 110-5 & 140-8". The FDA issued a decision of Substantially Equivalent on August 3, 1984. The device falls under product code DXO (Transducer, Pressure, Catheter Tip), a Class II device regulated under 21 CFR 870.2870. Camino Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 3, 1984
- Date Received
- May 17, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Transducer, Pressure, Catheter Tip
- Device Class
- Class II
- Regulation Number
- 870.2870
- Review Panel
- CV
- Submission Type