FDA 510(k) Applications Submitted by CHRIS HADLAND

FDA 510(k) Number Submission Date Device Name Applicant
K020082 01/10/2002 ERECAID CLASSIC SYSTEM; ERECAID ESTEEM MANUAL SYSTEM; ERECAID ESTEEM BATTERY SYSTEM ENDOCARE, INC.
K961450 04/15/1996 SCORE SOFTWARE NELLCOR PURITAN BENNETT, INC.
K972248 06/16/1997 NELLCOR PURITAN BENNETT GEMINI NELLCOR PURITAN BENNETT, INC.
K962516 06/27/1996 TAP ANTI-SNORING DEVICE NELLCOR PURITAN BENNETT, INC.
K953363 07/17/1995 OXIFLOW DIGITAL RECORDER EDENTEC CORP.
K964019 10/07/1996 MORPHEE PLUS ALPHA NELLCOR PURITAN BENNETT, INC.
K964516 11/05/1996 TAP NELLCOR PURITAN BENNETT, INC.
K964494 11/08/1996 SLEEPWIZARD NELLCOR PURITAN BENNETT, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact