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

FLUOROSCOPE BAND BAG

K Number: K861785 · Decision Jun 13, 1986
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
12
Review Days
36

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Basic Information

Device Name
FLUOROSCOPE BAND BAG
K Number
K861785
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Medi-Plast Intl., Inc.
Date Received
May 8, 1986
Decision Date
June 13, 1986
Product Code
JAA
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
JAA System, X-Ray, Fluoroscopic, Image-Intensified

Similar 510(k) Clearances

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

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Other Clearances by Medi-Plast Intl., Inc.

K Number Device Name
K954284 MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON)
K873588 10CC CONTROL SYRINGE
K863402 MEDI-PLAST DISPOSABLE MANIFOLD
K851489 ARTERIAL-VENOUS COMPRESSION DRESSING
K842136 STERILE PAN SET
K840021 OPERATING ROOM TRAY SET
K840022 HEART CATHETERIZATION TRAY SET
K811268 BOTTLE-TO-BOTTLE
K811234 I.V. BOTTLE (RIDGID)
K811233 I.V. PLASTIC BAG
Search all 12 clearances from Medi-Plast Intl., Inc. →