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

SANDMAN POCKET

K Number: K061996 · Decision Oct 3, 2006
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
160
Applicant Total
13
Review Days
81

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SANDMAN POCKET
K Number
K061996
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eb Neuro S.P.A.
Date Received
July 14, 2006
Decision Date
October 3, 2006
Product Code
MNR
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
Y

Classifications

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

Product Code Device Name
MNR Ventilatory Effort Recorder

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MNR), ordered by most recent decision date.

View all

Other Clearances by Eb Neuro S.P.A.

K Number Device Name
K242832 NExT Station; NExT Station Advanced
K242305 BE Plus PRO, Neurotravel LIGHT
K150220 STM 9000 Basic, STM 9000 Standard, STM 9000 Fast, STM 9000 Ultra-Fast
K142064 GALILEO NT
K133517 NEMUS 2 SYSTEM
K121996 BE PLUS LTM AMPLIFIER GWI AMPLIFIER
K093728 BE MICRO, TREA
K073415 NEMUS SYSTEM; NEMUS PC PERIPHERAL
K053606 BE PLUS / AURA-LTM64 AMPLIFIER
K041198 NIC36 AMPLIFIER
Search all 13 clearances from Eb Neuro S.P.A. →