510(k) K883668
K883668 is an FDA 510(k) premarket notification submitted by Exmoor Plastics , Ltd. for the device "SUNDERLAND NASAL TUBE". The FDA issued a decision of Substantially Equivalent on November 21, 1988. The device falls under product code BTQ (Airway, Nasopharyngeal), a Class I device regulated under 21 CFR 868.5100. Exmoor Plastics , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 21, 1988
- Date Received
- August 26, 1988
- 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