• FDA DYMISTA NDA 202236 approval records — 22 FDA documents, 848 pages
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FDA 510(k) K020530, EVANS SUB-Q, MODEL MC4206, by Evans Medical, Inc.

FDA 510(k) K020530, EVANS SUB-Q, MODEL MC4206, by Evans Medical, Inc.

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510(K) Number: K020530
Device Name: EVANS SUB-Q, MODEL MC4206
Manufacturer: Evans Medical, Inc.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 02/19/2002
Decision Date: 04/29/2002
Regulation Medical Specialty: General Hospital

Total pages: 99
Fully redacted pages: 26
Content pages: 73
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