FLEX BUBBLE TUBING— 510(k) K832865

Substantially Equivalent

Sheridan Catheter Corp.

FDA 510(k) clearance K832865 for FLEX BUBBLE TUBING, Substantially Equivalent on 1983-09-29. Applicant: Sheridan Catheter Corp.. Device class: 2.

Clearance details

Applicant: Sheridan Catheter Corp.
Product code: Code BYY
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1983-08-23
Decision date: 1983-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BYY

K960616 — VITAFLOW SUCTION/ASPIRATION TUBING SET1996-05-06
K960218 — CONNECTING TUBING1996-03-28
K955149 — MAXI-FLOW SUCTION HANDLE/THE REEL THING TUBING REEL1996-01-24
K955151 — MAXI-FLOW SUCTION TUBE/TOP GUN SUCTION IRRIGATOR1996-01-24
K955150 — MAXI-FLOW1996-01-23

More clearances from Sheridan Catheter Corp.

K922894 — LAZER-TRACH TRACHEAL TUBE1993-05-07
K897046 — LASER RESISTANT TRACHEAL TUBE1990-03-23
K890823 — ACCESSORY TO CLINICAL ELECTRONIC THERMOMETER1989-05-05
K884765 — CLINICAL ELECTRONIC THERMOMETERS1989-02-16
K882918 — KIM NASO-INTESTINAL TUBE1988-12-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.