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

INVIROSNAP SAFETY SYRINGE, MODELS 120006, 120007, 120008, 100080, 130022, 130023 AND 130024

K Number: K070203 · Decision Apr 23, 2007
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
161
Applicant Total
7
Review Days
91

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Basic Information

Device Name
INVIROSNAP SAFETY SYRINGE, MODELS 120006, 120007, 120008, 100080, 130022, 130023 AND 130024
K Number
K070203
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Inviro Medical Devices, Inc.
Date Received
January 22, 2007
Decision Date
April 23, 2007
Product Code
MEG
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
MEG Syringe, Antistick

Similar 510(k) Clearances

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Other Clearances by Inviro Medical Devices, Inc.

K Number Device Name
K101359 INVIROSTRIPE LUER LOCK SYRINGES (1, 3, 10, 20, 30 AND 60 ML)
K092413 INVIROSNAP 50 AND 100 UNIT INSULIN SAFETY SYRINGES
K092430 1 ML FIXED NEEDLE, 3 ML LUER LOCK, 5 ML LUER LOCK, 10 ML LUER LOCK, 20 ML LUERL LOCK SAFETY SYRINGES
K083851 INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022
K081436 INVIROSTRIPE 3ML, 5ML, 10ML LUER LOCK SYRINGES
K071307 INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003