FDA 510(k) clearance · back to tracker

Endomat Select (UP220)

KARL STORZ SE & CO. KG cleared K261706 on 2026-07-16, decision: substantially equivalent

K-number

K261706

Sponsor

KARL STORZ SE & CO. KG

Device

Endomat Select (UP220)

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-07-16

Product code

HIG

Advisory committee

Obstetrics/Gynecology

Medical specialty

Obstetrics/Gynecology

Regulation number

884.1700

Official FDA record

Open K261706on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

Use this as a predicate

Drop K261706 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

Try the sandbox

Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.