HEMASTAIN PHOSPHATE BUFFER— 510(k) K760487

Name: FDA 510(k) clearance K760487
Creator: U.S. Food and Drug Administration
Published: 1976-08-30

Substantially Equivalent

Geometric Data, Div. Smithkline Corp.

FDA 510(k) clearance K760487 for HEMASTAIN PHOSPHATE BUFFER, Substantially Equivalent on 1976-08-30. Applicant: Geometric Data, Div. Smithkline Corp.. Device class: 1.

Clearance details

Applicant: Geometric Data, Div. Smithkline Corp.
Product code: Code KQC
Device class: Class 1
Regulation: 21 CFR 864.1850
Advisory panel: Hematology
Date received: 1976-08-20
Decision date: 1976-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code KQC

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K882873 — FIELDTEX HEMATOXYLIN1988-07-28
K852843 — GENERAL DIAGNOSTICS COAG-A-MATE XC1985-08-13
K843619 — RETIC-SET1984-10-30
K841848 — RETIC-SET1984-05-31
K792550 — PONCEAU S STAIN SET1980-01-16

More clearances from Geometric Data, Div. Smithkline Corp.

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K841852 — AUTOLYZER 8001984-09-05
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K791041 — HEMATRAK ABNORMAL RECOGNITION1979-09-04
K790816 — HEMATRAK MODEL 4801979-07-17
K791108 — CONTEXT FILTER1979-07-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.