Home / 510(k) Clearances / K130736

510(k) K130736

BLOM-SINGER ADJUSTABLE BI-FIANGED FISTULA PROSTHESIS by Helix Medical, LLC — Product Code LRC

K130736 is an FDA 510(k) premarket notification submitted by Helix Medical, LLC for the device "BLOM-SINGER ADJUSTABLE BI-FIANGED FISTULA PROSTHESIS". The FDA issued a decision of Substantially Equivalent on December 17, 2013. The device falls under product code LRC (Instrument, Ent Manual Surgical), a Class I device regulated under 21 CFR 874.4420. Helix Medical, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 17, 2013
Date Received
March 18, 2013
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Ent Manual Surgical
Device Class
Class I
Regulation Number
874.4420
Review Panel
EN
Submission Type

Other clearances by Helix Medical, LLC

  • K131745 — BLOM-SINGER SEPTAL PERFORATION PROSTHESIS (September 17, 2013)
  • K093258 — BLOM-SINGER INDWELLING TEP OCCLUDER (March 3, 2010)
  • K082206 — BLOM-SINGER DUAL VALVE INDWELLING VOICE PROSTHESIS, MODELS DV-1600 SERIES, DV-20 (September 4, 2008)
  • K023259 — INHEALTH SOFT SLEEVE COLONOSCOPE SPLINT, MODEL CS1200 (December 26, 2002)
  • K991587 — BLOM-SINGER INDWELLING 2000 VOICE PROSTHESIS (June 25, 1999)
  • K945287 — INHEALTH BLOM-SINGER INDWELLING VALVED INSERT ACCESSORY DEVICE (December 9, 1994)
  • K945288 — INHEALTH BLOM-SINGER INDWELLING PLUG INSERT ACCESSORY DEVICE (December 2, 1994)
  • K932120 — BLOM-SINGER INDWELLING LOW PRESSURE VOICE PROSTHES (April 15, 1994)
  • K932163 — BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET (December 15, 1993)
  • K930105 — BLOM-SINGER LOW PRESSURE VOICE PROSTHESIS,P.I.D.S. (May 17, 1993)

Other clearances for product code LRC

  • K230258 — BB 8 Sinus Dilation Kit (May 25, 2023)
  • K212774 — VenSure LightGuide (February 4, 2022)
  • K201398 — SINUSPRIME Dilation System (October 15, 2020)
  • K201115 — Next Generation Balloon Dilation System (August 27, 2020)
  • K201472 — VenSure Balloon Device, VenSure Nav Balloon Device (August 26, 2020)
  • K181546 — Dillard Nasal Balloon Catheter (January 3, 2020)
  • K190525 — RELIEVA ULTIRRA Sinus Balloon Catheter (May 3, 2019)
  • K181838 — Sinusway Dilation System (December 20, 2018)
  • K172737 — MESIRE - Balloon Sinus Dilatation System (December 12, 2017)
  • K171687 — Relieva SpinPlus Nav Balloon Sinuplasty System (September 5, 2017)

FDA data resources