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FDA 510(k)

RODEL ELECTRODERM PADS

K-Number: K802658 · 1980-12-30

ApplicantRodel Products Corp.
Decision Date1980-12-30
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RODEL ELECTRODERM PADS is the device name listed in this FDA 510(k) record. The listed applicant is Rodel Products Corp.. It received FDA 510(k) clearance on 1980-12-30 under 510(k) number K802658. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RODEL ELECTRODERM PADS?

RODEL ELECTRODERM PADS is a medical device that received FDA 510(k) clearance on 1980-12-30. The listed applicant is Rodel Products Corp.. The 510(k) number is K802658.

When did RODEL ELECTRODERM PADS receive FDA 510(k) clearance?

RODEL ELECTRODERM PADS received FDA 510(k) clearance on 1980-12-30, under 510(k) number K802658.

Who is the listed applicant for RODEL ELECTRODERM PADS?

The FDA 510(k) record lists Rodel Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RODEL ELECTRODERM PADS?

The FDA product code for RODEL ELECTRODERM PADS is GYB.

Related Clinical Trials

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Other records listing Rodel Products Corp. 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.

K812299ELECTRO-SNAP

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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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