FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

PANPAC HSG CATHETER SET

K Number: K092983 · Decision Jun 7, 2010
Classifications
1
FEI Numbers
78
Registration Numbers
78
Same Product Code
86
Applicant Total
12
Review Days
252

Basic Information

Device Name
PANPAC HSG CATHETER SET
K Number
K092983
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Panpac Medical Corporation
Date Received
September 28, 2009
Decision Date
June 7, 2010
Product Code
LKF
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
LKF Cannula, Manipulator/Injector, Uterine

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Other Clearances by Panpac Medical Corporation

K Number Device Name
K173351 Panpac Flexi Shelf Pessary
K161106 PANPAC DISPOSABLE VACUUM CURETTES
K153422 Panpac Disposable Pessary Fitting Set
K132670 PANPAC INFLATABLE DOCUT PESSARY
K130087 PANPAC WORD/BARTHOLIN CATHETER
K130273 PANPAC VAGINAL DILATORS
K102898 BELLOTA SONOHYSTEROGRAPHY CATHETER WITH CERVICAL CONE, BELLOTA SONOHYSTEROGRAPHY CATHETER WITHOUT CERVICAL CONE
K092982 THE PANPAC SUCTION CURETTE
K092981 PANPAC VAGINAL PESSARY
K092984 PANPAC UTERINE INECTOR, MODEL UI-4.0, UI-2.0
Search all 12 clearances from Panpac Medical Corporation →