FLEX TUBE— 510(k) K881230

Substantially Equivalent

Intertech Resources, Inc.

FDA 510(k) clearance K881230 for FLEX TUBE, Substantially Equivalent on 1988-04-14. Applicant: Intertech Resources, Inc.. Device class: 1.

Clearance details

Applicant: Intertech Resources, Inc.
Product code: Code BZA
Device class: Class 1
Regulation: 21 CFR 868.5810
Advisory panel: Anesthesiology
Date received: 1988-03-22
Decision date: 1988-04-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Myers, FL, US

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