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

SPECTRA-LOR, 10 ML PLASTIC LOSS OF RESISTANCE SYRINGE, L/S, SPECTRA-LOR, 10ML PLASTIC LOSS OF RESISTANCE SYRINGE L/L

K Number: K081524 · Decision Jul 29, 2008
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
6
Review Days
57

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Basic Information

Device Name
SPECTRA-LOR, 10 ML PLASTIC LOSS OF RESISTANCE SYRINGE, L/S, SPECTRA-LOR, 10ML PLASTIC LOSS OF RESISTANCE SYRINGE L/L
K Number
K081524
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spectra Medical Devices, Inc.
Date Received
June 2, 2008
Decision Date
July 29, 2008
Product Code
FMF
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
FMF Syringe, Piston

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Other Clearances by Spectra Medical Devices, Inc.

K Number Device Name
K151069 SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle
K103740 SODIUM CHLORIDE INJECTION, 0.9%, USP 5 ML, 10 ML AMPULE
K082689 STERILE SODIUM CHLORIDE 0.9% FLUSH, 5ML, 10ML, AMPULE
K082580 SPECTRA GUIDEWIRE INTRODUCER NEEDLE
K082674 SPECTRA-GLASS LOR (LOSS OF RESISTANCE SYRINGE, 5CC METAL L/S OR L/L TIP, SPECTRA-GLASS LOR (LOSS OF RESISTANCE) SYRINGE