Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PENNINE LINK TUBING

K-Number: K853839 · 1985-10-07

Decision Date1985-10-07
Product Code
DecisionSubstantially Equivalent

Device Summary

PENNINE LINK TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Samco Industries, Inc.. It received FDA 510(k) clearance on 1985-10-07 under 510(k) number K853839. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENNINE LINK TUBING?

PENNINE LINK TUBING is a medical device that received FDA 510(k) clearance on 1985-10-07. The listed applicant is Samco Industries, Inc.. The 510(k) number is K853839.

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

PENNINE LINK TUBING received FDA 510(k) clearance on 1985-10-07, under 510(k) number K853839.

Who is the listed applicant for PENNINE LINK TUBING?

The FDA 510(k) record lists Samco Industries, Inc. 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.

Other records listing Samco Industries, Inc. 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.

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.

↑