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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.
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