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

MMG CONNECTIVE TUBING

K Number: K840838 · Decision Mar 30, 1984
Classifications
1
FEI Numbers
206
Registration Numbers
206
Same Product Code
26
Applicant Total
11
Review Days
35

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Basic Information

Device Name
MMG CONNECTIVE TUBING
K Number
K840838
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Medical Marketing Group
Date Received
February 24, 1984
Decision Date
March 30, 1984
Product Code
GAZ
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
GAZ Tubing, Noninvasive

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Other Clearances by Medical Marketing Group

K Number Device Name
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K874682 MMG CATHETER PLUG W/DRAINAGE TUBE COVER
K871999 MMG URO-SELF CATHETER
K863912 THE MMG 5 IN 1 CONNECTOR
K821168 DISPOSABLE URINARY LEGBAG W/STRAP
K811469 MMG URINARY DRAINAGE TUBING
K800694 MMG DISPOSABLE URINARY LEG BAG
K791847 ASPRI-LUKE
K790279 CATHETER, MMG LATEX EXTERNAL
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