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FDA 510(k)

SODIUM/POTASSIUM BUFFER SOLUTION

K-Number: K791692 · 1979-09-17

ApplicantHi Chem, Inc.
Decision Date1979-09-17
Product CodeCEM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SODIUM/POTASSIUM BUFFER SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Hi Chem, Inc.. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791692. The device is classified under product code CEM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SODIUM/POTASSIUM BUFFER SOLUTION?

SODIUM/POTASSIUM BUFFER SOLUTION is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Hi Chem, Inc.. The 510(k) number is K791692.

When did SODIUM/POTASSIUM BUFFER SOLUTION receive FDA 510(k) clearance?

SODIUM/POTASSIUM BUFFER SOLUTION received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791692.

Who is the listed applicant for SODIUM/POTASSIUM BUFFER SOLUTION?

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

What is the FDA product code for SODIUM/POTASSIUM BUFFER SOLUTION?

The FDA product code for SODIUM/POTASSIUM BUFFER SOLUTION is CEM.

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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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