INTRA-ALERT— 510(k) K781297

Substantially Equivalent

Pan-Tech Research, Inc.

FDA 510(k) clearance K781297 for INTRA-ALERT, Substantially Equivalent on 1978-10-25. Applicant: Pan-Tech Research, Inc.. Device class: 2.

Clearance details

Applicant: Pan-Tech Research, Inc.
Product code: Code FLN
Device class: Class 2
Regulation: 21 CFR 880.2420
Advisory panel: General Hospital
Date received: 1978-07-27
Decision date: 1978-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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