FDA 510(k) clearance · back to tracker
MEDICAL IMAGING WORKSTATION II (MIW II)
Cemco, Inc. cleared K941203 on 1994-06-27, decision: substantially equivalent
K-number
K941203
Sponsor
Cemco, Inc.
Device
MEDICAL IMAGING WORKSTATION II (MIW II)
Class
Class I
Decision
Substantially Equivalent
Decision date
1994-06-27
Product code
LMD
Advisory committee
Radiology
Medical specialty
Radiology
Regulation number
892.2020
Official FDA record
Open K941203on 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 K941203 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.