Atlas FDA

3M MICROBIAL PROFILE SYSTEM GRAM

FDA 510(k) clearance K791789 · decided 1979-11-16

Clearance details

K-number
K791789
Device name
3M MICROBIAL PROFILE SYSTEM GRAM
Applicant
3M Company
Decision
Substantially Equivalent
Date received
1979-09-14
Decision date
1979-11-16
Days to decision
63 days
Clearance type
Traditional
Product code
JSS
Device class
1
Regulation number
866.2660
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
White City, OR, US
Third-party review
No
Expedited review
No

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EK/P. AERUGINOSA PNA FISH (K081433)Advandx, Inc.2009-03-26
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ALAMAR BACTERIAL IDENTIFICATION TEST PANEL (K926002)Alamar Biosciences Laboratory, Inc.1993-09-23
API 20E/UNISCEPT 20E (K924814)Analytical Products, Inc.1993-03-11
CRYSTAL RAPID STOOL/ENTERIC ID SYSTEM (K926017)Becton Dickinson Microbiology Systems1993-03-11
CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM (K926018)Becton Dickinson Microbiology Systems1993-03-11

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S011)3M Company1994-11-28
CENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S010)3M Company1994-05-19
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S006)3M Company1992-12-31
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S009)3M Company1992-03-13
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S008)3M Company1992-01-28
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S007)3M Company1990-10-17
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S005)3M Company1990-03-08
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S004)3M Company1989-11-22