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FDA 510(k)

SORENSON SUBCLAVIAN CATHETER SSC-8

K-Number: K812326 · 1981-09-25

ApplicantSorensen Research
Decision Date1981-09-25
Product CodeLFJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SORENSON SUBCLAVIAN CATHETER SSC-8 is the device name listed in this FDA 510(k) record. The listed applicant is Sorensen Research. It received FDA 510(k) clearance on 1981-09-25 under 510(k) number K812326. The device is classified under product code LFJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORENSON SUBCLAVIAN CATHETER SSC-8?

SORENSON SUBCLAVIAN CATHETER SSC-8 is a medical device that received FDA 510(k) clearance on 1981-09-25. The listed applicant is Sorensen Research. The 510(k) number is K812326.

When did SORENSON SUBCLAVIAN CATHETER SSC-8 receive FDA 510(k) clearance?

SORENSON SUBCLAVIAN CATHETER SSC-8 received FDA 510(k) clearance on 1981-09-25, under 510(k) number K812326.

Who is the listed applicant for SORENSON SUBCLAVIAN CATHETER SSC-8?

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

What is the FDA product code for SORENSON SUBCLAVIAN CATHETER SSC-8?

The FDA product code for SORENSON SUBCLAVIAN CATHETER SSC-8 is LFJ.

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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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