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FDA 510(k)

EAGLE 2000 STERILIZER SERIES GAS/AERA

K-Number: K832945 · 1983-10-19

ApplicantAmsco Co.
Decision Date1983-10-19
Product CodeFLF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EAGLE 2000 STERILIZER SERIES GAS/AERA is the device name listed in this FDA 510(k) record. The listed applicant is Amsco Co.. It received FDA 510(k) clearance on 1983-10-19 under 510(k) number K832945. The device is classified under product code FLF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAGLE 2000 STERILIZER SERIES GAS/AERA?

EAGLE 2000 STERILIZER SERIES GAS/AERA is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Amsco Co.. The 510(k) number is K832945.

When did EAGLE 2000 STERILIZER SERIES GAS/AERA receive FDA 510(k) clearance?

EAGLE 2000 STERILIZER SERIES GAS/AERA received FDA 510(k) clearance on 1983-10-19, under 510(k) number K832945.

Who is the listed applicant for EAGLE 2000 STERILIZER SERIES GAS/AERA?

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

What is the FDA product code for EAGLE 2000 STERILIZER SERIES GAS/AERA?

The FDA product code for EAGLE 2000 STERILIZER SERIES GAS/AERA is FLF.

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Other records listing Amsco Co. as applicant

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Related Devices (Code: FLF)

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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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