Product code EWD— Unknown

FDA has cleared 14 devices under product code EWD between 1978 and 2002, filed by 11 applicant companies. No FDA device recalls reference this product code.

• 20021 clearance
• 19972 clearances
• 19962 clearances
• 19951 clearance
• 19931 clearance
• 19921 clearance
• 19911 clearance
• 19871 clearance
• 19821 clearance
• 19791 clearance
• 19782 clearances

• Virtual Corp.2 clearances
• Flents Products Co., Inc.2 clearances
• Doc'S Proplugs, Inc.2 clearances
• Santa Barbara Medco, Inc.1 clearance
• Mcghan Medical Corp.1 clearance
• Interview Medical Technology Corp.1 clearance
• Emtech Laboratories1 clearance
• Crown Delta Corp.1 clearance
• Bilson International, Inc.1 clearance
• Bentec Medical, Inc.1 clearance

• K020296 — ADULT SILICONE EAR PLUGS, MODELS # 68053, 68057Apothecary Products, Inc.·2002-06-25
• K972923 — SUPER SILIPLUGS EAR PLUGSInterview Medical Technology Corp.·1997-10-27
• K971517 — SILICONE PUTTY EAR PLUGSBentec Medical, Inc.·1997-06-02
• K962292 — HEARSAVEREmtech Laboratories·1996-10-29
• K960500 — THE VIRTUAL M-332Virtual Corp.·1996-04-03
• K945376 — DOC'S PROPLUGS EAR PLUGSDoc'S Proplugs, Inc.·1995-11-14
• K930203 — MODEL 322 CLINICAL AUDIOMETERVirtual Corp.·1993-07-08
• K915739 — #903 SILAFLEX IIFlents Products Co., Inc.·1992-06-30
• K910177 — SEAL-RITE SILICONE EAR PLUGFlents Products Co., Inc.·1991-06-24
• K862045 — DOC'S PROPLUGS EAR PLUGSDoc'S Proplugs, Inc.·1987-04-10
• K821187 — MEDCO CUSTOM EAR PROTECTOR MOLD KITSanta Barbara Medco, Inc.·1982-05-27
• K791608 — BILSOM PROPPBilson International, Inc.·1979-10-10
• K781907 — EAR STOPPLES FOR NOISE ATTENTIONCrown Delta Corp.·1978-11-22
• K781491 — PRO-MOLD, CUSTOM EARMcghan Medical Corp.·1978-09-27