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FDA 510(k)

SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311

K-Number: K101270 · 2011-02-10

ApplicantExcelsior Medical Corp.
Decision Date2011-02-10
Product CodeNGT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311 is the device name listed in this FDA 510(k) record. The listed applicant is Excelsior Medical Corp.. It received FDA 510(k) clearance on 2011-02-10 under 510(k) number K101270. The device is classified under product code NGT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311?

SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311 is a medical device that received FDA 510(k) clearance on 2011-02-10. The listed applicant is Excelsior Medical Corp.. The 510(k) number is K101270.

When did SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311 receive FDA 510(k) clearance?

SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311 received FDA 510(k) clearance on 2011-02-10, under 510(k) number K101270.

Who is the listed applicant for SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311?

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

What is the FDA product code for SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311?

The FDA product code for SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311 is NGT.

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Other records listing Excelsior Medical Corp. as applicant

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Related Devices (Code: NGT)

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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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