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FDA 510(k)

SORENSON CATALOG #IFL-120S

K-Number: K811228 · 1981-06-09

ApplicantSorensen Research
Decision Date1981-06-09
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SORENSON CATALOG #IFL-120S is the device name listed in this FDA 510(k) record. The listed applicant is Sorensen Research. It received FDA 510(k) clearance on 1981-06-09 under 510(k) number K811228. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORENSON CATALOG #IFL-120S?

SORENSON CATALOG #IFL-120S is a medical device that received FDA 510(k) clearance on 1981-06-09. The listed applicant is Sorensen Research. The 510(k) number is K811228.

When did SORENSON CATALOG #IFL-120S receive FDA 510(k) clearance?

SORENSON CATALOG #IFL-120S received FDA 510(k) clearance on 1981-06-09, under 510(k) number K811228.

Who is the listed applicant for SORENSON CATALOG #IFL-120S?

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 CATALOG #IFL-120S?

The FDA product code for SORENSON CATALOG #IFL-120S is CAC.

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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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