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FDA 510(k)

RECON-2 FLOW CONTROLLER

K-Number: K834260 · 1984-01-10

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

Device Summary

RECON-2 FLOW CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Precision Metering, Inc.. It received FDA 510(k) clearance on 1984-01-10 under 510(k) number K834260. The device is classified under product code CAX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECON-2 FLOW CONTROLLER?

RECON-2 FLOW CONTROLLER is a medical device that received FDA 510(k) clearance on 1984-01-10. The listed applicant is Precision Metering, Inc.. The 510(k) number is K834260.

When did RECON-2 FLOW CONTROLLER receive FDA 510(k) clearance?

RECON-2 FLOW CONTROLLER received FDA 510(k) clearance on 1984-01-10, under 510(k) number K834260.

Who is the listed applicant for RECON-2 FLOW CONTROLLER?

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

What is the FDA product code for RECON-2 FLOW CONTROLLER?

The FDA product code for RECON-2 FLOW CONTROLLER is CAX.

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.

Other records listing Precision Metering, Inc. as applicant

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: CAX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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