5.0 IOP & 7.5 IOP PROBES— 510(k) K853432

Substantially Equivalent

Diasonics, Inc.

FDA 510(k) clearance K853432 for 5.0 IOP & 7.5 IOP PROBES, Substantially Equivalent on 1986-02-07. Applicant: Diasonics, Inc.. Device class: 2.

Clearance details

Applicant: Diasonics, Inc.
Product code: Code GXW
Device class: Class 2
Regulation: 21 CFR 882.1240
Advisory panel: Neurology
Date received: 1985-08-15
Decision date: 1986-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milipitas, CA, US

Download summary PDF View on FDA.gov ↗

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