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BECKMAN R.PR CONTROL SERUM SET

FDA 510(k) clearance K812425 · decided 1981-09-23

Clearance details

K-number
K812425
Device name
BECKMAN R.PR CONTROL SERUM SET
Applicant
Beckman Instruments, Inc.
Decision
Substantially Equivalent
Date received
1981-08-24
Decision date
1981-09-23
Days to decision
30 days
Clearance type
Traditional
Product code
GMP
Device class
2
Regulation number
866.3820
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Mchenry, IL, 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
ADI SYPHILIS RPR LIQUID CONTROLS (K980638)Ampcor Diagnostics, Inc.1998-07-06
QUALITROL SYPHSERO CONTROL SET (K961998)Consolidated Technologies, Inc.1996-08-08
RPR LIQUID CONTROLS (K955143)Remel, L.P.1996-07-30
VISUWELL REAGIN TEST 960 TEST KIT (K885298)Allelix Diagnostics, Inc.1989-03-15
V-TREND RPRL CARD TEST (K875180)Texas Immunology, Inc.1988-02-04
VDRL CARBON ANTIGEN TEST S900500, S900250 & S90010 (K851504)Ncs Diagnostics, Inc.1985-08-19
RPR TEST REDITEST (K843741)Biokit USA, Inc.1984-10-25
CONTROL SERUMS FOR NONTREPONEMAL TEST (K810119)Hillside Acres, Inc.1981-02-09

Recalls involving this device

No recalls on record reference this clearance.