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FDA 510(k)

ACCU-FLO REGULATOR

K-Number: K865077 · 1987-02-10

ApplicantAlum-Ox, Inc.
Decision Date1987-02-10
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ACCU-FLO REGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Alum-Ox, Inc.. It received FDA 510(k) clearance on 1987-02-10 under 510(k) number K865077. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCU-FLO REGULATOR?

ACCU-FLO REGULATOR is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Alum-Ox, Inc.. The 510(k) number is K865077.

When did ACCU-FLO REGULATOR receive FDA 510(k) clearance?

ACCU-FLO REGULATOR received FDA 510(k) clearance on 1987-02-10, under 510(k) number K865077.

Who is the listed applicant for ACCU-FLO REGULATOR?

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

What is the FDA product code for ACCU-FLO REGULATOR?

The FDA product code for ACCU-FLO REGULATOR is CAN.

Related Clinical Trials

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Related Devices (Code: CAN)

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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