FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

SAFEPORT MANIFOLD (TM) (OR STOPCOCK)

K Number: K111016 · Decision Jun 9, 2011
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
16
Review Days
58

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Basic Information

Device Name
SAFEPORT MANIFOLD (TM) (OR STOPCOCK)
K Number
K111016
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elcam Medical Acal
Date Received
April 12, 2011
Decision Date
June 9, 2011
Product Code
FPA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FPA Set, Administration, Intravascular

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Other Clearances by Elcam Medical Acal

K Number Device Name
K231900 A-TAP (previously called Arthrotap)
K211204 SafePort(TM) Manifold (or Stopcock)
K190489 Elcam Stopcocks and Manifolds
K141254 ELCAM STOPCOCKS AND MANIFOLDS
K123084 DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD
K120253 ELCAM VITAL SIGNS WIRELESS SYSTEM (VSWS)
K120624 ELCAM DISPOSABLE INTEGRATED PRESSURE TRANSDUCER (DIPT)
K111467 FLEXI-Q DV AND DVR AUTO-INJECTORS
K100425 HASKAL TORQUE DEVICE
K082106 ELCAM ANTIMICROBIAL CLOSED STOPCOCKS (DSS AND TSS)
Search all 16 clearances from Elcam Medical Acal →