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FDA 510(k)

EAGLE PAC/VISIBLE SEAL

K-Number: K781699 · 1978-10-24

Decision Date1978-10-24
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EAGLE PAC/VISIBLE SEAL is the device name listed in this FDA 510(k) record. The listed applicant is American Sterilizer Co.. It received FDA 510(k) clearance on 1978-10-24 under 510(k) number K781699. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAGLE PAC/VISIBLE SEAL?

EAGLE PAC/VISIBLE SEAL is a medical device that received FDA 510(k) clearance on 1978-10-24. The listed applicant is American Sterilizer Co.. The 510(k) number is K781699.

When did EAGLE PAC/VISIBLE SEAL receive FDA 510(k) clearance?

EAGLE PAC/VISIBLE SEAL received FDA 510(k) clearance on 1978-10-24, under 510(k) number K781699.

Who is the listed applicant for EAGLE PAC/VISIBLE SEAL?

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

What is the FDA product code for EAGLE PAC/VISIBLE SEAL?

The FDA product code for EAGLE PAC/VISIBLE SEAL is KCT.

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 American Sterilizer 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.

View all 36 devices →

Related Devices (Code: KCT)

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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