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FDA 510(k)

PENNINE LINK YANKAUERS

K-Number: K844874 · 1985-06-06

ApplicantPennine Medical , Ltd.
Decision Date1985-06-06
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PENNINE LINK YANKAUERS is the device name listed in this FDA 510(k) record. The listed applicant is Pennine Medical , Ltd.. It received FDA 510(k) clearance on 1985-06-06 under 510(k) number K844874. 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 PENNINE LINK YANKAUERS?

PENNINE LINK YANKAUERS is a medical device that received FDA 510(k) clearance on 1985-06-06. The listed applicant is Pennine Medical , Ltd.. The 510(k) number is K844874.

When did PENNINE LINK YANKAUERS receive FDA 510(k) clearance?

PENNINE LINK YANKAUERS received FDA 510(k) clearance on 1985-06-06, under 510(k) number K844874.

Who is the listed applicant for PENNINE LINK YANKAUERS?

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

What is the FDA product code for PENNINE LINK YANKAUERS?

The FDA product code for PENNINE LINK YANKAUERS is GEA.

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Other records listing Pennine Medical , Ltd. 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.

K854443O'NEIL URINARY CATHETER INTRODUCERK852859PENNINE CONNECTING TUBINGK852081PENNINE OXYGEN LINK TUBINGK844876PENNINE NELATON CATHETERS SIZES 5,6,8,10,12,14,16,K852080PENNINE SUCTION CATHETERSK852079PENNINE DERBY YANKAUER

View all 8 devices →

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

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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