MINI LANCET-BLOOD LANCET— 510(k) K830705

Substantially Equivalent

Pharmaquest Corp.

FDA 510(k) clearance K830705 for MINI LANCET-BLOOD LANCET, Substantially Equivalent on 1983-04-08. Applicant: Pharmaquest Corp.. Device class: 1.

Clearance details

Applicant: Pharmaquest Corp.
Product code: Code FMA
Device class: Class 1
Regulation: 21 CFR 880.6230
Advisory panel: General Hospital
Date received: 1983-03-07
Decision date: 1983-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Pharmaquest Corp.

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K833236 — TELEPHONE TRANSMITTER T-10 EEG1983-11-29
K833880 — TELEPHONIC RECEIVER R-10 EEG1983-11-29
K822976 — HYPOCOUNT A1982-11-16
K822486 — HOME BLOOD GLUCOSE MONITOR1982-11-05

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