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FDA 510(k)

RNS STERILE DISPOSABLE PUNCTURE TRAY

K-Number: K955678 · 1996-02-21

Decision Date1996-02-21
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RNS STERILE DISPOSABLE PUNCTURE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Contour Fabricators of Florida, Inc.. It received FDA 510(k) clearance on 1996-02-21 under 510(k) number K955678. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RNS STERILE DISPOSABLE PUNCTURE TRAY?

RNS STERILE DISPOSABLE PUNCTURE TRAY is a medical device that received FDA 510(k) clearance on 1996-02-21. The listed applicant is Contour Fabricators of Florida, Inc.. The 510(k) number is K955678.

When did RNS STERILE DISPOSABLE PUNCTURE TRAY receive FDA 510(k) clearance?

RNS STERILE DISPOSABLE PUNCTURE TRAY received FDA 510(k) clearance on 1996-02-21, under 510(k) number K955678.

Who is the listed applicant for RNS STERILE DISPOSABLE PUNCTURE TRAY?

The FDA 510(k) record lists Contour Fabricators of Florida, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RNS STERILE DISPOSABLE PUNCTURE TRAY?

The FDA product code for RNS STERILE DISPOSABLE PUNCTURE TRAY is FRG.

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 Contour Fabricators of Florida, 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.

View all 18 devices →

Related Devices (Code: FRG)

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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