FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SNAP MODEL 5

K Number: K992322 · Decision Feb 2, 2000
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
160
Applicant Total
6
Review Days
205

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Basic Information

Device Name
SNAP MODEL 5
K Number
K992322
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Snap Laboratories, LLC
Date Received
July 12, 1999
Decision Date
February 2, 2000
Product Code
MNR
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MNR Ventilatory Effort Recorder

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Other Clearances by Snap Laboratories, LLC

K Number Device Name
K080321 SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM
K002095 SNAP MODEL 6
K984169 DIGI-SNAP
K971184 OXI-SNAP
K944524 SNAP TESTING DEVICE