Atlas FDA

SAS SALMONELLA H K ANTISERUM

FDA 510(k) clearance K955206 · decided 1996-02-02

Clearance details

K-number
K955206
Device name
SAS SALMONELLA H K ANTISERUM
Applicant
Sa Scientific, Inc.
Decision
Substantially Equivalent
Date received
1995-11-14
Decision date
1996-02-02
Days to decision
80 days
Clearance type
Traditional
Product code
GNC
Device class
2
Regulation number
866.3550
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
San Antonio, TX, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VISTA ANTIGEN SALMONELLA O GROUP C (K972388)Lee Laboratories, Inc.1997-08-25
VISTA ANTIGEN SALMONELLA O GROUP A (K972387)Lee Laboratories, Inc.1997-08-25
VISTA ANTIGEN SALMONELLA H B (K972391)Lee Laboratories, Inc.1997-08-25
VISTA ANTIGEN SALMONELLA H D (K972389)Lee Laboratories, Inc.1997-08-25
VISTA ANTIGEN SALMONELLA H A (K972392)Lee Laboratories, Inc.1997-08-25
VISTA ANTIGEN SALMONELLA H C (K972390)Lee Laboratories, Inc.1997-08-25
VISTA ANTIGEN SALMONELLA O GROUP B (K972386)Lee Laboratories, Inc.1997-08-25
VISTA ANTIGEN SALMONELLA O GROUP D (K972395)Lee Laboratories, Inc.1997-08-25
SAS SPICER-EDWARDS 3 ANTISERUM (K955225)Sa Scientific, Inc.1996-02-13
SAS SPICER-EDWARDS 2 ANTISERUM (K955224)Sa Scientific, Inc.1996-02-13
SAS SPICER-EDWARDS 4 ANTISERUM (K955226)Sa Scientific, Inc.1996-02-13
SAS SPICER-EDWARDS 1 ANTISERUM (K955223)Sa Scientific, Inc.1996-02-13

Recalls involving this device

No recalls on record reference this clearance.