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FDA 510(k)

EAGLE DS

K-Number: K895164 · 1989-11-17

ApplicantAmerican Sterilizer Co.
Decision Date1989-11-17
Product CodeECG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EAGLE DS 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 1989-11-17 under 510(k) number K895164. The device is classified under product code ECG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAGLE DS?

EAGLE DS is a medical device that received FDA 510(k) clearance on 1989-11-17. The listed applicant is American Sterilizer Co.. The 510(k) number is K895164.

When did EAGLE DS receive FDA 510(k) clearance?

EAGLE DS received FDA 510(k) clearance on 1989-11-17, under 510(k) number K895164.

Who is the listed applicant for EAGLE DS?

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 DS?

The FDA product code for EAGLE DS is ECG.

Related Clinical Trials

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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.

K943288AMSCO SQ240 SURGICAL LIGHTK931872THE EAGLE 3017 100% ETHYLENE OXIDE STERILIZERK922485CHEMDI-VHP CHEMICAL INDICATORK930493QUANTUM 3080 SURGICAL TABLEK905816ORTHOVISION TABLEK896674AMSCO QUANTUM LIGHT

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Related Devices (Code: ECG)

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.

K843234CITOMAT AUTOCLAVESLic-OrthionK811237MAGNETIC RETENTION UNITUniversiti MalayaK810977ENDODONTIC POST SYSTEMSPreat Corp.K790290NEY EQUI-HINGEDeringer-Ney, Inc.K790078BAR & RIDER, SCREWS, TUBESEurodent, Inc.K771266STEAM STERILIZERAmsco Hospital Products Co.

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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