510(k) K901078
K901078 is an FDA 510(k) premarket notification submitted by L H M Ent., Inc. for the device "SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN 0.9% SALINE". The FDA issued a decision of Substantially Equivalent on May 18, 1990. The device falls under product code BTO (Tube, Tracheostomy (W/Wo Connector)), a Class II device regulated under 21 CFR 868.5800. L H M Ent., Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 18, 1990
- Date Received
- March 7, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tube, Tracheostomy (W/Wo Connector)
- Device Class
- Class II
- Regulation Number
- 868.5800
- Review Panel
- AN
- Submission Type