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

APPLE MEDICAL ONE-TOUCH UTERINE SAMPLER

K Number: K000026 · Decision Mar 31, 2000
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
41
Applicant Total
9
Review Days
86

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Basic Information

Device Name
APPLE MEDICAL ONE-TOUCH UTERINE SAMPLER
K Number
K000026
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1175
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Apple Medical Corp.
Date Received
January 5, 2000
Decision Date
March 31, 2000
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 Apple Medical Corp.

K Number Device Name
K061651 FISCHER CONE BIOPSY EXCISOR, MODELS 900-150, 151, 152, 154, 155, 157 AND 158
K050256 APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTOR
K041131 APPLE MEDICAL OB MOBIUS ELASTIC RETRACTOR
K014005 APPLE MEDICAL MOBIUS ELASTIC RETRACTOR
K970788 PNEUMO-MATIC INSUFFLATION NEEDLE
K961460 LWEET CONE BIOPSY INSTRUMENT
K952841 THE ASSISTANT
K941506 URETERAL ILLUMINATOR