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510(k) K905052

BIVONA ENDOTRACHEAL TUBE STYLET by Bivona Medical Technologies — Product Code BSR

K905052 is an FDA 510(k) premarket notification submitted by Bivona Medical Technologies for the device "BIVONA ENDOTRACHEAL TUBE STYLET". The FDA issued a decision of Substantially Equivalent on April 2, 1991. The device falls under product code BSR (Stylet, Tracheal Tube), a Class I device regulated under 21 CFR 868.5790. Bivona Medical Technologies has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 2, 1991
Date Received
November 8, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stylet, Tracheal Tube
Device Class
Class I
Regulation Number
868.5790
Review Panel
AN
Submission Type

Other clearances by Bivona Medical Technologies

  • K952700 — SUPERSLICK (October 31, 1995)
  • K942025 — BURGET NASAL STENT (October 27, 1995)
  • K944178 — BIVONA FLEXTEND PEDIATRIC & NEONATAL TRACHEOSTROMY TUBES (October 27, 1994)
  • K935053 — BIVONA NASAL TURBINATE STENT (July 1, 1994)
  • K933398 — BIVONA ILLUMINATED ENDOTRACHEAL TUBE (October 6, 1993)
  • K931749 — BIVONA(R) ICU ENDOTRACHEAL TUBE (August 10, 1993)
  • K922665 — BIVONA HYPERFLEX TRACHEOSTOMY TUBE (January 7, 1993)
  • K923878 — BIVONA CUSTOMIZED TRACHEOSTOMY TUBES (December 29, 1992)
  • K920604 — BIVONA TRACHEAL T-TUBE STENT (July 27, 1992)
  • K915761 — BIVONA-COLORADO VOICE PROSTHESIS (June 29, 1992)

Other clearances for product code BSR

  • K162729 — Aintree Intubation Catheter, Arndt Airway Exchange Catheter Set, Cook Airway Exc (August 11, 2017)
  • K962361 — TRACHLIGHT STYLET AND TRACHEAL LIGHTWAND (September 5, 1996)
  • K954771 — TRACHLIGHT STYLET & TRACHEAL LIGHTWAND (ORIGINAL APPLICATION NAME: STYLETT & TRA (May 9, 1996)
  • K943104 — MOLLOY INTUBATING STYLETTE (April 18, 1996)
  • K955238 — RUSCH SCHROEDER ENDOTRACHEAL TUBE STYLE (February 6, 1996)
  • K953677 — LIGHTED FLEXGUIDE (MODIFICATION) (August 25, 1995)
  • K952100 — RUSCH ENDOTRACHEAL TUBE STYLET (August 8, 1995)
  • K952266 — SCHROEDER ORAL/NASAL DIRECTIONAL STYLETTE (June 12, 1995)
  • K950713 — AIRGUIDE STYLETTE (May 17, 1995)
  • K950380 — FLEXTITIP STYLETTE (February 10, 1995)

FDA data resources