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FDA 510(k)

LIPASE CALIBRATOR

K-Number: K943704 · 1994-09-14

ApplicantThe DU Pont Co.
Decision Date1994-09-14
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIPASE CALIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is The DU Pont Co.. It received FDA 510(k) clearance on 1994-09-14 under 510(k) number K943704. 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 LIPASE CALIBRATOR?

LIPASE CALIBRATOR is a medical device that received FDA 510(k) clearance on 1994-09-14. The listed applicant is The DU Pont Co.. The 510(k) number is K943704.

When did LIPASE CALIBRATOR receive FDA 510(k) clearance?

LIPASE CALIBRATOR received FDA 510(k) clearance on 1994-09-14, under 510(k) number K943704.

Who is the listed applicant for LIPASE CALIBRATOR?

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

What is the FDA product code for LIPASE CALIBRATOR?

The FDA product code for LIPASE CALIBRATOR is JIT.

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Other records listing The DU Pont 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.

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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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