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FDA 510(k)

ELECTRO-SNAP

K-Number: K812299 · 1981-09-11

ApplicantRodel Products Corp.
Decision Date1981-09-11
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRO-SNAP 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 1981-09-11 under 510(k) number K812299. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-SNAP?

ELECTRO-SNAP is a medical device that received FDA 510(k) clearance on 1981-09-11. The listed applicant is Rodel Products Corp.. The 510(k) number is K812299.

When did ELECTRO-SNAP receive FDA 510(k) clearance?

ELECTRO-SNAP received FDA 510(k) clearance on 1981-09-11, under 510(k) number K812299.

Who is the listed applicant for ELECTRO-SNAP?

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 ELECTRO-SNAP?

The FDA product code for ELECTRO-SNAP is GXY.

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 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.

K802658RODEL ELECTRODERM PADS

Related Devices (Code: GXY)

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

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