VITALMAX 4000/MINIPACK 3100/3000— 510(k) K951226

Name: FDA 510(k) clearance K951226
Creator: U.S. Food and Drug Administration
Published: 1996-11-21

Substantially Equivalent

Pace Tech, Inc.

FDA 510(k) clearance K951226 for VITALMAX 4000/MINIPACK 3100/3000, Substantially Equivalent on 1996-11-21. Applicant: Pace Tech, Inc.. Device class: 2.

Clearance details

Applicant: Pace Tech, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1995-03-20
Decision date: 1996-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Pace Tech, Inc.

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K953795 — VITALMAX 41001996-07-01
K944541 — HANDYPACK 911SC1995-02-22
K945385 — VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 3001995-01-31
K925701 — MINIPACK 911-STC1994-08-11
K934385 — MINIPACK 3100/3000 MODIFICATION1994-08-10

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