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

THE PANPAC SUCTION CURETTE

K Number: K092982 · Decision Jul 26, 2010
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
41
Applicant Total
12
Review Days
301

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Basic Information

Device Name
THE PANPAC SUCTION CURETTE
K Number
K092982
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1175
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Panpac Medical Corporation
Date Received
September 28, 2009
Decision Date
July 26, 2010
Product Code
HHK
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
HHK Curette, Suction, Endometrial (And Accessories)

Similar 510(k) Clearances

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

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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
K092981 PANPAC VAGINAL PESSARY
K092983 PANPAC HSG CATHETER SET
K092984 PANPAC UTERINE INECTOR, MODEL UI-4.0, UI-2.0
Search all 12 clearances from Panpac Medical Corporation →