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FDA 510(k)

POTASSIUM DILUENT

K-Number: K830636 · 1983-04-05

ApplicantShaban Mfg. Co.
Decision Date1983-04-05
Product CodeJIH
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

POTASSIUM DILUENT is the device name listed in this FDA 510(k) record. The listed applicant is Shaban Mfg. Co.. It received FDA 510(k) clearance on 1983-04-05 under 510(k) number K830636. The device is classified under product code JIH. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POTASSIUM DILUENT?

POTASSIUM DILUENT is a medical device that received FDA 510(k) clearance on 1983-04-05. The listed applicant is Shaban Mfg. Co.. The 510(k) number is K830636.

When did POTASSIUM DILUENT receive FDA 510(k) clearance?

POTASSIUM DILUENT received FDA 510(k) clearance on 1983-04-05, under 510(k) number K830636.

Who is the listed applicant for POTASSIUM DILUENT?

The FDA 510(k) record lists Shaban Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POTASSIUM DILUENT?

The FDA product code for POTASSIUM DILUENT is JIH.

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Other records listing Shaban Mfg. Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K853621REPLACEMENT PUMP TUBINGK850157CANNULAS FOR HEMA-TEK I & KK SLIDE STAINERSK850333PUMP TUBE SETS FOR HEMA-TEK I & II SLIDE STAINERSK844781MEMBRANE KITS-KC1, CO2 & 02 FOR INSTRUMENT-LABK844235CHLORIDE STANDARDK842656REPLACEMENT PARTS NOVA ELECTROLYTE ANAL

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Related Devices (Code: JIH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K050338MODIFICATION TO: INSTAREAD LITHIUM SYSTEMAkers Biosciences, Inc.K031579INSTAREAD LITHIUM SYSTEMAkers Laboratories, Inc.K011033DIMENSION LITHIUM (LI) FLEX REAGENT CARTRIDGE, MODEL DF 132Dade Behring, Inc.K934106KODAK EKTACHEM DTSC II SLIDES (LI)Eastman Kodak CompanyK924488KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES (LI)Eastman Kodak CompanyK921403MODEL 654 ANALYZERCiba Corning Diagnostics Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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