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FDA 510(k)

EEI SLUSH PAN DRAPE

K-Number: K001994 · 2000-08-04

ApplicantEagle Endoscopic, Inc.
Decision Date2000-08-04
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EEI SLUSH PAN DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Eagle Endoscopic, Inc.. It received FDA 510(k) clearance on 2000-08-04 under 510(k) number K001994. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EEI SLUSH PAN DRAPE?

EEI SLUSH PAN DRAPE is a medical device that received FDA 510(k) clearance on 2000-08-04. The listed applicant is Eagle Endoscopic, Inc.. The 510(k) number is K001994.

When did EEI SLUSH PAN DRAPE receive FDA 510(k) clearance?

EEI SLUSH PAN DRAPE received FDA 510(k) clearance on 2000-08-04, under 510(k) number K001994.

Who is the listed applicant for EEI SLUSH PAN DRAPE?

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

What is the FDA product code for EEI SLUSH PAN DRAPE?

The FDA product code for EEI SLUSH PAN DRAPE is KKX.

Related Clinical Trials

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Other records listing Eagle Endoscopic, 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.

K001264EAGLE ENDO SPECIMEN RETRIEVAL BAG

Related Devices (Code: KKX)

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.

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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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