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FDA 510(k)

PENNINE CONNECTING TUBING

K-Number: K852859 · 1985-07-30

ApplicantPennine Medical , Ltd.
Decision Date1985-07-30
Product Code
DecisionSubstantially Equivalent

Device Summary

PENNINE CONNECTING TUBING 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 1985-07-30 under 510(k) number K852859. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENNINE CONNECTING TUBING?

PENNINE CONNECTING TUBING is a medical device that received FDA 510(k) clearance on 1985-07-30. The listed applicant is Pennine Medical , Ltd.. The 510(k) number is K852859.

When did PENNINE CONNECTING TUBING receive FDA 510(k) clearance?

PENNINE CONNECTING TUBING received FDA 510(k) clearance on 1985-07-30, under 510(k) number K852859.

Who is the listed applicant for PENNINE CONNECTING TUBING?

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

Related Clinical Trials

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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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 INTRODUCERK852081PENNINE OXYGEN LINK TUBINGK844874PENNINE LINK YANKAUERSK844876PENNINE NELATON CATHETERS SIZES 5,6,8,10,12,14,16,K852080PENNINE SUCTION CATHETERSK852079PENNINE DERBY YANKAUER

View all 8 devices →

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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