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FDA 510(k)

ARTICULATING PAPER

K-Number: K771011 · 1977-06-20

ApplicantParker Laboratories, Inc.
Decision Date1977-06-20
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 Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1977-06-20 under 510(k) number K771011. 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 1977-06-20. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K771011.

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

ARTICULATING PAPER received FDA 510(k) clearance on 1977-06-20, under 510(k) number K771011.

Who is the listed applicant for ARTICULATING PAPER?

The FDA 510(k) record lists Parker Laboratories, 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.

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Other records listing Parker Laboratories, 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.

K233965UltraDrape UGPIV Barrier and Securement (34-15)K953673ECLIPSE PROBE COVERK921695ULTRA COVER ULTRASOUND TRANSDUCER PROBE COVERSK864556AQUALUBE(TM)K861239ACRYLIC SOLDERK855167DYNA SYSTEM

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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.K832647ARTICULATING PAPERArdent Intl., Inc.

Official Source

View on FDA Database →

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

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