510(k) K900456
K900456 is an FDA 510(k) premarket notification submitted by Polamedco, Inc. for the device "POLAMEDCO NASOPAHARYNGEAL AIRWAY". The FDA issued a decision of Substantially Equivalent on April 19, 1990. The device falls under product code BTQ (Airway, Nasopharyngeal), a Class I device regulated under 21 CFR 868.5100. Polamedco, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 19, 1990
- Date Received
- January 30, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Airway, Nasopharyngeal
- Device Class
- Class I
- Regulation Number
- 868.5100
- Review Panel
- AN
- Submission Type