The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Smith & Nephew Operative Hysteroscope, Model 7209208; Smith & Nephew Continuous Flow Sheath, Model 8105224.
Device ID | K013870 |
510k Number | K013870 |
Device Name: | SMITH & NEPHEW OPERATIVE HYSTEROSCOPE, MODEL 7209208; SMITH & NEPHEW CONTINUOUS FLOW SHEATH, MODEL 8105224 |
Classification | Hysteroscope (and Accessories) |
Applicant | SMITH & NEPHEW, INC. 160 DASCOMB RD. Andover, MA 01810 |
Contact | Janice Haselton |
Correspondent | Janice Haselton SMITH & NEPHEW, INC. 160 DASCOMB RD. Andover, MA 01810 |
Product Code | HIH |
CFR Regulation Number | 884.1690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-11-21 |
Decision Date | 2002-01-17 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10884521746664 | K013870 | 000 |
10884521744141 | K013870 | 000 |