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

RDP-2

K Number: K961922 · Decision Aug 9, 1996
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
12
Review Days
84

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Basic Information

Device Name
RDP-2
K Number
K961922
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ranfac, Corp.
Date Received
May 17, 1996
Decision Date
August 9, 1996
Product Code
HET
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
HET Laparoscope, Gynecologic (And Accessories)

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K150563 Marrow Cellution Bone Marrow Aspiration Needle
K140991 RANFAC ASPIRATION NEEDLE WITH ADJUSTABLE GUIDE
K131157 RANFAC BONE MARROW ASPIRATION NEEDLE
K031344 RANFAC GOLDENBERG SNARECOIL SOFT TISSUE BIOPSY (GSS) NEEDLE
K012224 SINGLE ACTION BIOPSY NEEDLE, MODEL RCBS: XX GAUGE, XX LENGTH, XX THROW
K951090 INTRODUCER
K930474 NEEDLE, PNEUMOPERITONEUM, SPRING LOADED
K864139 RANFAC CUT BIOPSY NEEDLE
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