510(k) K915786
K915786 is an FDA 510(k) premarket notification submitted by Helix Medical, Inc. for the device "BLOM-SINGER HUMID/FIL SYST INHEALTH IN-LINE HUMID.". The FDA issued a decision of Substantially Equivalent on June 30, 1992. The device falls under product code BYD (Condenser, Heat And Moisture (Artificial Nose)), a Class I device regulated under 21 CFR 868.5375. Helix Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 30, 1992
- Date Received
- December 24, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Condenser, Heat And Moisture (Artificial Nose)
- Device Class
- Class I
- Regulation Number
- 868.5375
- Review Panel
- AN
- Submission Type