INFRA-LINK— 510(k) K926029

Substantially Equivalent

Zygo Industries, Inc.

FDA 510(k) clearance K926029 for INFRA-LINK, Substantially Equivalent on 1993-03-26. Applicant: Zygo Industries, Inc.. Device class: 2.

Clearance details

Applicant: Zygo Industries, Inc.
Product code: Code IQA
Device class: Class 2
Regulation: 21 CFR 890.3725
Advisory panel: Physical Medicine
Date received: 1992-12-01
Decision date: 1993-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IQA

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K943244 — DEUCE1995-09-11
K944585 — SCANNING DIRECTOR1995-02-21

More clearances from Zygo Industries, Inc.

K924013 — MACAW1993-03-04
K924014 — SECRETARY1993-03-04
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K924030 — SCRIBE1993-03-04
K862766 — EPISON, ALERTING SYSTEM FOR EPILEPTICS1987-03-13

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