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FDA 510(k)

ACA LIPASE VERIFIERS

K-Number: K772285 · 1978-01-06

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1978-01-06
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACA LIPASE VERIFIERS 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 1978-01-06 under 510(k) number K772285. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACA LIPASE VERIFIERS?

ACA LIPASE VERIFIERS is a medical device that received FDA 510(k) clearance on 1978-01-06. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K772285.

When did ACA LIPASE VERIFIERS receive FDA 510(k) clearance?

ACA LIPASE VERIFIERS received FDA 510(k) clearance on 1978-01-06, under 510(k) number K772285.

Who is the listed applicant for ACA LIPASE VERIFIERS?

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 ACA LIPASE VERIFIERS?

The FDA product code for ACA LIPASE VERIFIERS is JJX.

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

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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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