510(k) K894586
K894586 is an FDA 510(k) premarket notification submitted by Dale Medical Products, Inc. for the device "DALE I.V. IDENTIFIER; PRODUCT #1125". The FDA issued a decision of Substantially Equivalent on August 15, 1989. The device falls under product code KMK (Device, Intravascular Catheter Securement), a Class I device regulated under 21 CFR 880.5210. Dale Medical Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 15, 1989
- Date Received
- July 24, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Intravascular Catheter Securement
- Device Class
- Class I
- Regulation Number
- 880.5210
- Review Panel
- HO
- Submission Type