Eagle Pac/Visible Seal

FDA 510(k) K781699 · American Sterilizer Co.

Substantially Equivalent

510(k) numberK781699

Submission

Device name
Eagle Pac/Visible Seal
Applicant
American Sterilizer Co.
Walker, MI, US
Received
October 11, 1978
Decision date
October 24, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KCT – Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6850
Specialty
General Hospital

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K922485Chemdi-Vhp Chemical IndicatorJOJ · Traditional 09/29/1993SE
K930493Quantum 3080 Surgical TableFQO · Traditional 06/22/1993SE
K905816Orthovision TableJEB · Traditional 03/06/1991SE
K896674Amsco Quantum LightFSY · Traditional 01/03/1990SE
K895164Eagle DSECG · Traditional 11/17/1989SE
K882660General Surgical Table and AccessoriesFQO · Traditional 07/25/1988SE
K880198Gemini Surgical LightFSS · Traditional 02/10/1988SE
K864846Radiographic - Leg SectionKQS · Traditional 12/24/1986SE

Questions and answers

When was Eagle Pac/Visible Seal cleared by the FDA?

Eagle Pac/Visible Seal (K781699) received a 510(k) decision of Substantially Equivalent on October 24, 1978, 13 days after the submission was received.

What is the product code of K781699?

The FDA product code is KCT – Sterilization Wrap Containers, Trays, Cassettes & Other Accessories, a Class II (moderate risk) device regulated under 21 CFR 880.6850.