Skip to content
MedTekOSTry the sandbox

FDA 510(k) clearance · back to tracker

Laser Speckle Imaging System (RFLSI CZW)

Rwd Life Science Co., Ltd. cleared K233076 on 2024-05-28, decision: substantially equivalent

K-number

K233076

Sponsor

Rwd Life Science Co., Ltd.

Device

Laser Speckle Imaging System (RFLSI CZW)

Class

Class II

Decision

Substantially Equivalent

Decision date

2024-05-28

Product code

DPT

Advisory committee

Cardiovascular

Medical specialty

Cardiovascular

Regulation number

870.2120

Official FDA record

Open K233076on 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 K233076 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.