VITALMAX 4100— 510(k) K953795

Substantially Equivalent

Pace Tech, Inc.

FDA 510(k) clearance K953795 for VITALMAX 4100, Substantially Equivalent on 1996-07-01. Applicant: Pace Tech, Inc.. Device class: 2.

Clearance details

Applicant: Pace Tech, Inc.
Product code: Code CBS
Device class: Class 2
Regulation: 21 CFR 868.1620
Advisory panel: Anesthesiology
Date received: 1995-08-14
Decision date: 1996-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

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Recent devices under product code CBS

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K950101 — RAMS (RANDOM ACCESS MASS SPECTROMETER) M-200 RESPIRATORY GAS MONITOR1995-03-21
K943458 — AS/3 AIRWAY MODULE1995-02-14

More clearances from Pace Tech, Inc.

K951226 — VITALMAX 4000/MINIPACK 3100/30001996-11-21
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.