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FDA 510(k)

DISPOSABLE YANKAUER SUCTION TUBE

K-Number: K904881 · 1991-03-06

ApplicantPilling Medical S.A.
Decision Date1991-03-06
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE YANKAUER SUCTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Medical S.A.. It received FDA 510(k) clearance on 1991-03-06 under 510(k) number K904881. The device is classified under product code GEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE YANKAUER SUCTION TUBE?

DISPOSABLE YANKAUER SUCTION TUBE is a medical device that received FDA 510(k) clearance on 1991-03-06. The listed applicant is Pilling Medical S.A.. The 510(k) number is K904881.

When did DISPOSABLE YANKAUER SUCTION TUBE receive FDA 510(k) clearance?

DISPOSABLE YANKAUER SUCTION TUBE received FDA 510(k) clearance on 1991-03-06, under 510(k) number K904881.

Who is the listed applicant for DISPOSABLE YANKAUER SUCTION TUBE?

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

What is the FDA product code for DISPOSABLE YANKAUER SUCTION TUBE?

The FDA product code for DISPOSABLE YANKAUER SUCTION TUBE is GEA.

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Related Devices (Code: GEA)

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.

K003965MRI SAFE INSTRUMENTSAesculap, Inc.K982472GENICON TROCARGenicon, LCK954599CONMED TROGARD ELECTRONIC TROCAR SYSTEMConmedcorpK922460ORIGIN SECONDARY CANNULA AND TROCAROrigin Medsystems, Inc.K920110ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVEETHICON, Inc.K911262DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCERETHICON, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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