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FDA 510(k)

IN LINE VALVE CATALOG NO. 2000A

K-Number: K854965 · 1986-02-21

Decision Date1986-02-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IN LINE VALVE CATALOG NO. 2000A is the device name listed in this FDA 510(k) record. The listed applicant is Rao Medical Devices, Inc.. It received FDA 510(k) clearance on 1986-02-21 under 510(k) number K854965. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IN LINE VALVE CATALOG NO. 2000A?

IN LINE VALVE CATALOG NO. 2000A is a medical device that received FDA 510(k) clearance on 1986-02-21. The listed applicant is Rao Medical Devices, Inc.. The 510(k) number is K854965.

When did IN LINE VALVE CATALOG NO. 2000A receive FDA 510(k) clearance?

IN LINE VALVE CATALOG NO. 2000A received FDA 510(k) clearance on 1986-02-21, under 510(k) number K854965.

Who is the listed applicant for IN LINE VALVE CATALOG NO. 2000A?

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

What is the FDA product code for IN LINE VALVE CATALOG NO. 2000A?

The FDA product code for IN LINE VALVE CATALOG NO. 2000A is FPA.

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 Rao Medical Devices, 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: FPA)

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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