LANGHAM OCULAR BLOOD FLOW (OBF) TONOGRAPH/TONOMETER MODEL 201— 510(k) K010998

Name: FDA 510(k) clearance K010998
Creator: U.S. Food and Drug Administration
Published: 2001-06-27

Unknown

Langham Ophthalmic Technologies

FDA 510(k) clearance K010998 for LANGHAM OCULAR BLOOD FLOW (OBF) TONOGRAPH/TONOMETER MODEL 201, Unknown on 2001-06-27. Applicant: Langham Ophthalmic Technologies. Device class: 2.

Clearance details

Applicant: Langham Ophthalmic Technologies
Product code: Code HKX
Device class: Class 2
Regulation: 21 CFR 886.1930
Advisory panel: Ophthalmic
Date received: 2001-04-03
Decision date: 2001-06-27
Decision: Unknown
Clearance type: Traditional
Location: Timonium, MD, US

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