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FDA 510(k)

TUBULAR HOLLOW FIBER MEMBRANE

K-Number: K841476 · 1984-08-03

ApplicantAmerican Bentley
Decision Date1984-08-03
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TUBULAR HOLLOW FIBER MEMBRANE is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1984-08-03 under 510(k) number K841476. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBULAR HOLLOW FIBER MEMBRANE?

TUBULAR HOLLOW FIBER MEMBRANE is a medical device that received FDA 510(k) clearance on 1984-08-03. The listed applicant is American Bentley. The 510(k) number is K841476.

When did TUBULAR HOLLOW FIBER MEMBRANE receive FDA 510(k) clearance?

TUBULAR HOLLOW FIBER MEMBRANE received FDA 510(k) clearance on 1984-08-03, under 510(k) number K841476.

Who is the listed applicant for TUBULAR HOLLOW FIBER MEMBRANE?

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

What is the FDA product code for TUBULAR HOLLOW FIBER MEMBRANE?

The FDA product code for TUBULAR HOLLOW FIBER MEMBRANE is DTZ.

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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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