INFUSION PUMP— 510(k) K882830

Substantially Equivalent

Pemlab Corp.

FDA 510(k) clearance K882830 for INFUSION PUMP, Substantially Equivalent on 1988-12-30. Applicant: Pemlab Corp.. Device class: 2.

Clearance details

Applicant: Pemlab Corp.
Product code: Code LZF
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1988-07-08
Decision date: 1988-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, 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.