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

EMODREN GUIDE NEEDLE FOR DRAINAGE TUBE & EMODREN

K Number: K853296 · Decision Aug 15, 1985
Classifications
1
FEI Numbers
174
Registration Numbers
174
Same Product Code
23
Applicant Total
14
Review Days
9

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Basic Information

Device Name
EMODREN GUIDE NEEDLE FOR DRAINAGE TUBE & EMODREN
K Number
K853296
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Parexel Intl. Corp.
Date Received
August 6, 1985
Decision Date
August 15, 1985
Product Code
BYY
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
BYY Tube, Aspirating, Flexible, Connecting

Similar 510(k) Clearances

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Other Clearances by Parexel Intl. Corp.

K Number Device Name
K900385 ACTA METRA/ACTA GNOSIS FIRMWARE PACKAGE
K904901 L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC
K904902 SMA 26 TRANSDUCER
K884800 ACTA GENOS ELECTROCARDIOGRAPH
K862414 FUJI CR IMAGING PLATE
K864519 PHILIPS COMPUTED RADIOGRAPHY SYSTEM (PCR)
K862415 TYPE 633 COMPUTED RADIOGRAPHY (CR) FILM
K862416 FTI 100 MEDICAL THERMAL IMAGER
K853295 EMODREN EXCHANGEABLE PLASTIC BELLOWS
K851322 PERSONAL C3 3-CHANNEL ELECTROCARDIOGRAPH
Search all 14 clearances from Parexel Intl. Corp. →