510(k) K880487
K880487 is an FDA 510(k) premarket notification submitted by Neotech Products, Inc. for the device "NEOTECH MECONIUM ASPIRATOR (STERILE)". The FDA issued a decision of Substantially Equivalent on May 6, 1988. The device falls under product code BTR (Tube, Tracheal (W/Wo Connector)), a Class II device regulated under 21 CFR 868.5730. Neotech Products, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 6, 1988
- Date Received
- February 4, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tube, Tracheal (W/Wo Connector)
- Device Class
- Class II
- Regulation Number
- 868.5730
- Review Panel
- AN
- Submission Type