# K121261: Asap Muitiscope

- Pathway: 510(k) (Traditional)
- Applicant: Asap Endoscopic Products GmbH
- Decided: Jan 8, 2013 after 257 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K991794 (1999). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051827: Joimax Endoscope/Multiscope, Thessys Foraminoscope/Multiscope, Thessys Laminoscope/Multiscope, Joimax GmbH (2005) Summary page 1.
- K061246: Endoscopic Spine System, Arthro Kinetics, Inc. (2006) Summary page 1.
- K083552: Maxmorespine Tom Stick, Hoogland Spine Products, GmbH (2009) Summary page 1.

## Indications for use
The asap multiscope is intended to visualize the inside of the patient through a cannulated incision for diagnostic and surgical procedures, such as arthroplasty, nucleotomy. discectomy, and foraminotomy.

Source page: https://510kreport.com/device/K121261
Methodology: https://510kreport.com/methodology