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FDA 510(k)

ULTRAFLOW

K-Number: K871901 · 1987-06-01

ApplicantCustom Industries, Inc.
Decision Date1987-06-01
Product CodeFZH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ULTRAFLOW is the device name listed in this FDA 510(k) record. The listed applicant is Custom Industries, Inc.. It received FDA 510(k) clearance on 1987-06-01 under 510(k) number K871901. The device is classified under product code FZH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRAFLOW?

ULTRAFLOW is a medical device that received FDA 510(k) clearance on 1987-06-01. The listed applicant is Custom Industries, Inc.. The 510(k) number is K871901.

When did ULTRAFLOW receive FDA 510(k) clearance?

ULTRAFLOW received FDA 510(k) clearance on 1987-06-01, under 510(k) number K871901.

Who is the listed applicant for ULTRAFLOW?

The FDA 510(k) record lists Custom Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRAFLOW?

The FDA product code for ULTRAFLOW is FZH.

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Related Devices (Code: FZH)

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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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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