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FDA 510(k)

ARTICULATING PAPER

K-Number: K832647 · 1984-02-21

ApplicantArdent Intl., Inc.
Decision Date1984-02-21
Product CodeEFH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ARTICULATING PAPER is the device name listed in this FDA 510(k) record. The listed applicant is Ardent Intl., Inc.. It received FDA 510(k) clearance on 1984-02-21 under 510(k) number K832647. The device is classified under product code EFH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTICULATING PAPER?

ARTICULATING PAPER is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Ardent Intl., Inc.. The 510(k) number is K832647.

When did ARTICULATING PAPER receive FDA 510(k) clearance?

ARTICULATING PAPER received FDA 510(k) clearance on 1984-02-21, under 510(k) number K832647.

Who is the listed applicant for ARTICULATING PAPER?

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

What is the FDA product code for ARTICULATING PAPER?

The FDA product code for ARTICULATING PAPER is EFH.

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.

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Other records listing Ardent Intl., 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.

K864300SILIVA EJECTOR/ORAL CAVITY EVACUATORK842512EXACTA-FILM

Related Devices (Code: EFH)

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.

K965026PFINGST PRESSURE PASTEPfingst & Co., Inc.K912632OCCLUDEPascal Co., Inc.K911259HYDENTPascal Co., Inc.K864572FIXTECTORProdent Intl., Inc.K870032REVISED T-SCAN SYSTEMSentek, Inc.K833132MUCOSAL ADJUSTMENT PASTE LIQUID SPRAYMyo-Tronics Research, Inc.

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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