FDA 510(k) clearance · back to tracker
EPISTAT-II NASAL CATHETER
Merocel Corp. cleared K943718 on 1994-09-16, decision: substantially equivalent
K-number
K943718
Sponsor
Merocel Corp.
Device
EPISTAT-II NASAL CATHETER
Class
Class I
Decision
Substantially Equivalent
Decision date
1994-09-16
Product code
EMX
Advisory committee
Ear, Nose, Throat
Medical specialty
Ear, Nose, Throat
Regulation number
874.4100
Official FDA record
Open K943718on 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 K943718 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 sandboxSource
Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.