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FDA 510(k)

DROPPER, CEPTI-SEAL LAVTOPHENOL

K-Number: K781868 · 1978-11-22

Decision Date1978-11-22
Product CodeKEQ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

DROPPER, CEPTI-SEAL LAVTOPHENOL is the device name listed in this FDA 510(k) record. The listed applicant is Marion Laboratories, Inc.. It received FDA 510(k) clearance on 1978-11-22 under 510(k) number K781868. The device is classified under product code KEQ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DROPPER, CEPTI-SEAL LAVTOPHENOL?

DROPPER, CEPTI-SEAL LAVTOPHENOL is a medical device that received FDA 510(k) clearance on 1978-11-22. The listed applicant is Marion Laboratories, Inc.. The 510(k) number is K781868.

When did DROPPER, CEPTI-SEAL LAVTOPHENOL receive FDA 510(k) clearance?

DROPPER, CEPTI-SEAL LAVTOPHENOL received FDA 510(k) clearance on 1978-11-22, under 510(k) number K781868.

Who is the listed applicant for DROPPER, CEPTI-SEAL LAVTOPHENOL?

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

What is the FDA product code for DROPPER, CEPTI-SEAL LAVTOPHENOL?

The FDA product code for DROPPER, CEPTI-SEAL LAVTOPHENOL is KEQ.

Related Clinical Trials

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.

Other records listing Marion Laboratories, Inc. 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.

View all 38 devices →

Related Devices (Code: KEQ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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