RYDER LACRIMAL INTUBATIONSET— 510(k) K962151

Name: FDA 510(k) clearance K962151
Creator: U.S. Food and Drug Administration
Published: 1996-09-18

Substantially Equivalent

Ryder Intl. Corp.

FDA 510(k) clearance K962151 for RYDER LACRIMAL INTUBATIONSET, Substantially Equivalent on 1996-09-18. Applicant: Ryder Intl. Corp.. Device class: Unclassified.

Clearance details

Applicant: Ryder Intl. Corp.
Product code: Code OKS
Device class: Unclassified
Advisory panel: Unknown
Date received: 1996-06-04
Decision date: 1996-09-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arab, AL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OKS

view all

K201892 — Ritleng®+ and Ritleng®+ PVP2021-03-11
K201606 — LacriJet®2020-12-18
K170247 — Lacriflow CL2017-04-18
K161373 — Nunchaku2016-11-03
K160710 — Oasis Lacrimal Intubation Set2016-05-13

More clearances from Ryder Intl. Corp.

view all

K962611 — BARD EAGLE INFLATION DEVICE1996-10-21
K953522 — USCI IDEAL PTCA KIT1996-04-17
K920064 — OPTI-LENS CONTACT LENS CASE1992-03-04
K915082 — OPTI-LENS(TM) CONTACT LENS CASE1992-01-13
K881981 — ASSIST(TM) ASEPTIC SYRINGE IRRIGATION SYSTEM1988-08-02

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