LEONARD TUBE— 510(k) K892334

Substantially Equivalent

Surgidyne, Inc.

FDA 510(k) clearance K892334 for LEONARD TUBE, Substantially Equivalent on 1989-05-31. Applicant: Surgidyne, Inc.. Device class: 2.

Clearance details

Applicant: Surgidyne, Inc.
Product code: Code KDH
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1989-04-05
Decision date: 1989-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Inver Grove Heights, MN, US

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More clearances from Surgidyne, Inc.

K883582 — VARIDYNE MODEL 250 SUCTION DRAINAGE SYSTEM1988-10-03
K864822 — VARIDYNE 550, MODELS 12E,12M,24E & 24M SUCTION SYS1987-01-15
K860030 — SURGIDYNE VARIDYNE, MODEL 140-2I & MODEL 140-2ID1986-02-12
K852180 — SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC.1985-07-01
K850634 — SURGIDYNE SURGIFLO C.W.S. DRAIN PRODUCTS1985-06-28

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