Atlas FDA

MOPSO BUFFER

FDA 510(k) clearance K792574 · decided 1980-01-21

Clearance details

K-number
K792574
Device name
MOPSO BUFFER
Applicant
Electrophoresis Corp. of America
Decision
Substantially Equivalent
Date received
1979-12-13
Decision date
1980-01-21
Days to decision
39 days
Clearance type
Traditional
Product code
JCC
Device class
1
Regulation number
864.4010
Medical specialty
Pathology
Advisory committee
Pathology
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
SCOTTS TAP WATER SUBSTITUTE (K842918)E K Ind., Inc.1984-09-11
WRIGHT STAIN BUFFER (K842914)E K Ind., Inc.1984-09-07
SCOTTS TAP WATER SUBSTITUTE 7 (K841423)Reagent Laboratory, Inc.1984-05-22
PHOSPHATE BUFFERED SALINE (1X) (K811791)Dutchland Laboratories, Inc.1981-08-25
CITRATE BUFFER (K811251)Bioscientific1981-05-21
SMAC SYSTEM (K770508)Mid Tech, Inc.1977-05-09

Recalls involving this device

No recalls on record reference this clearance.