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FDA 510(k)

PANASONIC MODEL EW-213

K-Number: K831151 · 1983-08-11

ApplicantPanasonic Co. Div. Matsu Elec. Corp. America
Decision Date1983-08-11
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PANASONIC MODEL EW-213 is the device name listed in this FDA 510(k) record. The listed applicant is Panasonic Co. Div. Matsu Elec. Corp. America. It received FDA 510(k) clearance on 1983-08-11 under 510(k) number K831151. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PANASONIC MODEL EW-213?

PANASONIC MODEL EW-213 is a medical device that received FDA 510(k) clearance on 1983-08-11. The listed applicant is Panasonic Co. Div. Matsu Elec. Corp. America. The 510(k) number is K831151.

When did PANASONIC MODEL EW-213 receive FDA 510(k) clearance?

PANASONIC MODEL EW-213 received FDA 510(k) clearance on 1983-08-11, under 510(k) number K831151.

Who is the listed applicant for PANASONIC MODEL EW-213?

The FDA 510(k) record lists Panasonic Co. Div. Matsu Elec. Corp. America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PANASONIC MODEL EW-213?

The FDA product code for PANASONIC MODEL EW-213 is DXN.

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Other records listing Panasonic Co. Div. Matsu Elec. Corp. America as applicant

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Related Devices (Code: DXN)

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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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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