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FDA 510(k)

SLO-FLO 40AL ADJUST-FLOW REGULATOR

K-Number: K834061 · 1984-01-10

Decision Date1984-01-10
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SLO-FLO 40AL ADJUST-FLOW REGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is S.L.O. Health Products, Inc.. It received FDA 510(k) clearance on 1984-01-10 under 510(k) number K834061. 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 SLO-FLO 40AL ADJUST-FLOW REGULATOR?

SLO-FLO 40AL ADJUST-FLOW REGULATOR is a medical device that received FDA 510(k) clearance on 1984-01-10. The listed applicant is S.L.O. Health Products, Inc.. The 510(k) number is K834061.

When did SLO-FLO 40AL ADJUST-FLOW REGULATOR receive FDA 510(k) clearance?

SLO-FLO 40AL ADJUST-FLOW REGULATOR received FDA 510(k) clearance on 1984-01-10, under 510(k) number K834061.

Who is the listed applicant for SLO-FLO 40AL ADJUST-FLOW REGULATOR?

The FDA 510(k) record lists S.L.O. Health Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SLO-FLO 40AL ADJUST-FLOW REGULATOR?

The FDA product code for SLO-FLO 40AL ADJUST-FLOW REGULATOR is CAN.

Related Clinical Trials

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.

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.

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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