# K014207: Reposable Instrument System, Models MF001-MF083

- Pathway: 510(k) (Traditional)
- Applicant: Aesculap, Inc.
- Decided: Mar 21, 2002 after 90 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K932648 (1993). 8 ancestors in all.
8 later devices descend from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K980758: 3 MM Selec-Tip Laparoscopic Scissors, Microline Pentax, Inc. (1998). Our OCR of the scanned summary read K580758, which is not a number in FDA’s lists. Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “3 MM Select-Tip Laparoscopic Instrument System”.
- K970826: Selecta-Tip Laparoscopic Scissors, Microline Pentax, Inc. (1997) Summary page 1.
- K926203: Endoscopic Scissors (Disposable/Reusable Shafts), Weck Endoscopy (1993) Summary page 1.

## Most influential descendants
- K063485: Logic Laparoscopic Scissors (2006), 7 descendants of its own
- K090583: Endoscopic Monopolar Scissors, Models Ems-235, Ems-165 (2009), 4 descendants of its own
- K141058: Ensizor Endoscopic Scissors (2014), 3 descendants of its own
- K150939: Ensizor Endoscopic Scissors (2015), 2 descendants of its own
- K100109: Logiflex Laparoscopic Band Positioning Device (2010), 1 descendant of its own

## Indications for use
Aesculap's Reposable Instrument System is designed to cut, dissect, manipulate and/or cauterize various tissue during endoscopic/laproscopic general, vascular, gynecological, and thoracic surgical procedures.

Source page: https://510kreport.com/device/K014207
Methodology: https://510kreport.com/methodology