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FDA 510(k)

RAIL CLAMP EXTENSION PIECE

K-Number: K864459 · 1986-12-01

Decision Date1986-12-01
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RAIL CLAMP EXTENSION PIECE is the device name listed in this FDA 510(k) record. The listed applicant is American Container Technology, Inc.. It received FDA 510(k) clearance on 1986-12-01 under 510(k) number K864459. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAIL CLAMP EXTENSION PIECE?

RAIL CLAMP EXTENSION PIECE is a medical device that received FDA 510(k) clearance on 1986-12-01. The listed applicant is American Container Technology, Inc.. The 510(k) number is K864459.

When did RAIL CLAMP EXTENSION PIECE receive FDA 510(k) clearance?

RAIL CLAMP EXTENSION PIECE received FDA 510(k) clearance on 1986-12-01, under 510(k) number K864459.

Who is the listed applicant for RAIL CLAMP EXTENSION PIECE?

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

What is the FDA product code for RAIL CLAMP EXTENSION PIECE?

The FDA product code for RAIL CLAMP EXTENSION PIECE is FWZ.

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 American Container Technology, 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: FWZ)

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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