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FDA 510(k)

ENDO-SCRUB/ENDO-SCRUB 2

K-Number: K982594 · 1998-08-27

ApplicantXomed, Inc.
Decision Date1998-08-27
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ENDO-SCRUB/ENDO-SCRUB 2 is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1998-08-27 under 510(k) number K982594. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO-SCRUB/ENDO-SCRUB 2?

ENDO-SCRUB/ENDO-SCRUB 2 is a medical device that received FDA 510(k) clearance on 1998-08-27. The listed applicant is Xomed, Inc.. The 510(k) number is K982594.

When did ENDO-SCRUB/ENDO-SCRUB 2 receive FDA 510(k) clearance?

ENDO-SCRUB/ENDO-SCRUB 2 received FDA 510(k) clearance on 1998-08-27, under 510(k) number K982594.

Who is the listed applicant for ENDO-SCRUB/ENDO-SCRUB 2?

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

What is the FDA product code for ENDO-SCRUB/ENDO-SCRUB 2?

The FDA product code for ENDO-SCRUB/ENDO-SCRUB 2 is EOB.

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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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