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FDA 510(k)

KNAI SODIUM POTASSIUM ANALYZER

K-Number: K830805 · 1983-04-08

ApplicantRadiometer America, Inc.
Decision Date1983-04-08
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

KNAI SODIUM POTASSIUM ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Radiometer America, Inc.. It received FDA 510(k) clearance on 1983-04-08 under 510(k) number K830805. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNAI SODIUM POTASSIUM ANALYZER?

KNAI SODIUM POTASSIUM ANALYZER is a medical device that received FDA 510(k) clearance on 1983-04-08. The listed applicant is Radiometer America, Inc.. The 510(k) number is K830805.

When did KNAI SODIUM POTASSIUM ANALYZER receive FDA 510(k) clearance?

KNAI SODIUM POTASSIUM ANALYZER received FDA 510(k) clearance on 1983-04-08, under 510(k) number K830805.

Who is the listed applicant for KNAI SODIUM POTASSIUM ANALYZER?

The FDA 510(k) record lists Radiometer America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KNAI SODIUM POTASSIUM ANALYZER?

The FDA product code for KNAI SODIUM POTASSIUM ANALYZER is JSG.

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Other records listing Radiometer America, Inc. as applicant

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Related Devices (Code: JSG)

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.

K882495THIOGLYCOLLATE BROTH W/VITA. K & HEMIN - #T3007Lakewood Biochemical Co., Inc.K881558TRYPTOSE AGARAcumedia Manufacturers, Inc.K881550OF BASAL MEDIUMAcumedia Manufacturers, Inc.K881557TRYPTONEAcumedia Manufacturers, Inc.K881564TRYPTOSE BLOOD AGAR BASE W/YEAST EXTRACTAcumedia Manufacturers, Inc.K881533BLOOD AGAR BASE NO. 2Acumedia Manufacturers, Inc.

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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