FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)

K Number: K241987 · Decision Aug 2, 2024
Classifications
1
FEI Numbers
135
Registration Numbers
135
Same Product Code
170
Applicant Total
9
Review Days
25

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Basic Information

Device Name
Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)
K Number
K241987
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
884.1690
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Guangzhou Red Pine Medical Instrument Co., Ltd.
Date Received
July 8, 2024
Decision Date
August 2, 2024
Product Code
HIH
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
HIH Hysteroscope (And Accessories)

Similar 510(k) Clearances

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

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Other Clearances by Guangzhou Red Pine Medical Instrument Co., Ltd.

K Number Device Name
K251951 Single-Use Video Flexible Ureterorenoscope (RP-U-C03R9, RP-U-C03R3, RP-U-C03S9, RP-U-C03S3); Endoscopic Video Image Processor (RP-IPD-V2000EF); Endoscopic Video Image Processor (RP-IPD-V1000F)
K252176 Single-Use Video Flexible Cysto-Nephroscope (RP-U-C01F, RP-U-C01FS)
K243321 Endoscopic Video Image Processor (RP-IPD-V1000F)
K241500 Endoscopic Video Image Processor (RP-IPD-V2000EF); Single-Use Video Flexible Cysto-Nephroscope (RP-U-C01F, RP-U-C01FS)
K240663 Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S)
K232043 Endoscopic Video Image Processor (RP-IPD-V2000A, RP-IPD-V2000B, RP-IPD-V2000C, RP-IPD-V2000D), Single-Use Video Gastroscope (RP-GI-G02A, RP-GI-G02B), Single-Use Video Colonoscope (RP-GI-C02A, RP-GI-C02B)
K232003 Endoscopic Video Image Processor, Single-Use Video Hysteroscope
K221158 Single-Use Video Flexible Ureterorenoscope System