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FDA 510(k)

RION ELECTRO-PALATOGRAPH MODEL DP-01

K-Number: K802870 · 1980-12-17

ApplicantKindel & Anderson
Decision Date1980-12-17
Product CodeLEZ
DecisionSubstantially Equivalent

Device Summary

RION ELECTRO-PALATOGRAPH MODEL DP-01 is the device name listed in this FDA 510(k) record. The listed applicant is Kindel & Anderson. It received FDA 510(k) clearance on 1980-12-17 under 510(k) number K802870. The device is classified under product code LEZ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RION ELECTRO-PALATOGRAPH MODEL DP-01?

RION ELECTRO-PALATOGRAPH MODEL DP-01 is a medical device that received FDA 510(k) clearance on 1980-12-17. The listed applicant is Kindel & Anderson. The 510(k) number is K802870.

When did RION ELECTRO-PALATOGRAPH MODEL DP-01 receive FDA 510(k) clearance?

RION ELECTRO-PALATOGRAPH MODEL DP-01 received FDA 510(k) clearance on 1980-12-17, under 510(k) number K802870.

Who is the listed applicant for RION ELECTRO-PALATOGRAPH MODEL DP-01?

The FDA 510(k) record lists Kindel & Anderson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RION ELECTRO-PALATOGRAPH MODEL DP-01?

The FDA product code for RION ELECTRO-PALATOGRAPH MODEL DP-01 is LEZ.

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 Kindel & Anderson 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.

K823384HEARING AID HB-72 RIONETK823383HEARING AID HB-33 RIONETK802812RIONET HEARING AID

Related Devices (Code: LEZ)

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.

K091682LSVT C OR LSVT COMPANION, MODEL V.1Lsvt Global, LLCK982396VISIVOX, MODEL V-2Rsq, LLC

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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