FDA 510(k) clearance · back to tracker

DEKNATEL(TM) PLEUR-EVAC(R) THORACIC CATHETER

Deknatel, Inc. cleared K925243 on 1994-07-27, decision: substantially equivalent

K-number

K925243

Sponsor

Deknatel, Inc.

Device

DEKNATEL(TM) PLEUR-EVAC(R) THORACIC CATHETER

Class

Class I

Decision

Substantially Equivalent

Decision date

1994-07-27

Product code

GBX

Advisory committee

General, Plastic Surgery

Medical specialty

General, Plastic Surgery

Regulation number

878.4200

Official FDA record

Open K925243on 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 K925243 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.

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Source

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