OPHTA SIL (R), LACHRYMAL INTUBATION SETS— 510(k) K911109

Name: FDA 510(k) clearance K911109
Creator: U.S. Food and Drug Administration
Published: 1991-05-01

Substantially Equivalent

G.W.B. Intl., Ltd.

FDA 510(k) clearance K911109 for OPHTA SIL (R), LACHRYMAL INTUBATION SETS, Substantially Equivalent on 1991-05-01. Applicant: G.W.B. Intl., Ltd.. Device class: Unclassified.

Clearance details

Applicant: G.W.B. Intl., Ltd.
Product code: Code OKS
Device class: Unclassified
Advisory panel: Unknown
Date received: 1991-03-04
Decision date: 1991-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sudbury, MA, US

Download summary PDF View on FDA.gov ↗

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K940508 — OPHTA SIL (RITLENG PROBE AND LACRIMAL INTUBATION SET)1994-05-04
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Data sourced from openFDA. This site is unofficial and independent of the FDA.