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FDA 510(k)

URINARY/CEBROSPINAL FLUID PROTEIN CALIBRATOR

K-Number: K934843 · 1994-03-11

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1994-03-11
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URINARY/CEBROSPINAL FLUID PROTEIN CALIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1994-03-11 under 510(k) number K934843. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINARY/CEBROSPINAL FLUID PROTEIN CALIBRATOR?

URINARY/CEBROSPINAL FLUID PROTEIN CALIBRATOR is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K934843.

When did URINARY/CEBROSPINAL FLUID PROTEIN CALIBRATOR receive FDA 510(k) clearance?

URINARY/CEBROSPINAL FLUID PROTEIN CALIBRATOR received FDA 510(k) clearance on 1994-03-11, under 510(k) number K934843.

Who is the listed applicant for URINARY/CEBROSPINAL FLUID PROTEIN CALIBRATOR?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URINARY/CEBROSPINAL FLUID PROTEIN CALIBRATOR?

The FDA product code for URINARY/CEBROSPINAL FLUID PROTEIN CALIBRATOR is JIT.

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Other records listing E.I. Dupont DE Nemours & Co., Inc. as applicant

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Related Devices (Code: JIT)

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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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