REVISED BATTERY CHARGER— 510(k) K790689

Name: FDA 510(k) clearance K790689
Creator: U.S. Food and Drug Administration
Published: 1979-05-29

Substantially Equivalent

Vickers America Medical Corp.

FDA 510(k) clearance K790689 for REVISED BATTERY CHARGER, Substantially Equivalent on 1979-05-29. Applicant: Vickers America Medical Corp.. Device class: 2.

Clearance details

Applicant: Vickers America Medical Corp.
Product code: Code FPL
Device class: Class 2
Regulation: 21 CFR 880.5410
Advisory panel: General Hospital
Date received: 1979-04-10
Decision date: 1979-05-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FPL

view all

K220742 — NxtGen Infant Transport Incubator2022-07-15
K161918 — SREE MRI Transport Incubator2017-03-03
K141565 — GLOBE-TROTTER GT54002014-09-10
K123937 — ATOM TRANSCAPSULE V-7072013-05-23
K103523 — 185A+ TRANSPORT INCUBATOR WITH MASIMO PULSEOX, 185A+ TRANSPORT INCUBATOR WITH NELLCOR PULSEOX2011-05-11

More clearances from Vickers America Medical Corp.

view all

K840823 — TREONIC C301984-03-23
K831838 — LABORATORY DATA MGMT SYSTEM SDMS1984-01-24
K830748 — RESUSCITAIRE1983-06-22
K830936 — TREONIC IP51983-04-12
K813239 — OXYGENAIRE NURING INCUBATOR1982-01-28

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