Atlas FDA

LO-ION

FDA 510(k) clearance K790973 · decided 1979-06-15

Clearance details

K-number
K790973
Device name
LO-ION
Applicant
Gamma Biologicals, Inc.
Decision
Substantially Equivalent
Date received
1979-05-23
Decision date
1979-06-15
Days to decision
23 days
Clearance type
Traditional
Product code
KSG
Device class
2
Regulation number
864.9600
Medical specialty
Hematology
Advisory committee
Hematology
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
ELUTION SOLUTION (K812565)Biological Corp. of America1981-10-23
EM-X (K812222)Biological Corp. of America1981-09-23
PENTEX BOVINE ALBUMIN 30% SOLUTION (K800943)Miles Laboratories, Inc.1980-05-08
BOVINE ALBUMIN 22% & 30% SOLUTIONS (K800189)Gotham Biologics, Inc.1980-02-13
ORTHO ANTIBODY ENHANCEMENT SOLUTION (K791791)Ortho Diagnostics, Inc.1979-10-11
LOW IONIC STRENGTH SOLUTION (LISS) (K791113)Hyland Therapeutic Div., Travenol Laboratories1979-06-28
DADE LOW IONIC STRENGTH SOLUITION (LISS) (K790776)Dade, Baxter Travenol Diagnostics, Inc.1979-05-23
LISS REAGENT (K790498)Fisher Scientific Co., LLC1979-04-03
ORTHO LOW IONIC SOLUTION (K781435)Ortho Diagnostics, Inc.1978-09-14
EM-V (K781397)Biological Corp. of America1978-09-14
LOW IIONIC STRENGTH SOLUTION (K780413)Pfizer, Inc.1978-04-24
SPECT RIM (LISS) (K780556)Bd Becton Dickinson Vacutainer Systems Preanalytic1978-04-24

Recalls involving this device

No recalls on record reference this clearance.