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FDA 510(k)

EVEN-TEMP. CAPACITIVE ADHESIVE PAD

K-Number: K831299 · 1983-06-02

Decision Date1983-06-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EVEN-TEMP. CAPACITIVE ADHESIVE PAD is the device name listed in this FDA 510(k) record. The listed applicant is Delta Medical Electronics, Inc.. It received FDA 510(k) clearance on 1983-06-02 under 510(k) number K831299. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVEN-TEMP. CAPACITIVE ADHESIVE PAD?

EVEN-TEMP. CAPACITIVE ADHESIVE PAD is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is Delta Medical Electronics, Inc.. The 510(k) number is K831299.

When did EVEN-TEMP. CAPACITIVE ADHESIVE PAD receive FDA 510(k) clearance?

EVEN-TEMP. CAPACITIVE ADHESIVE PAD received FDA 510(k) clearance on 1983-06-02, under 510(k) number K831299.

Who is the listed applicant for EVEN-TEMP. CAPACITIVE ADHESIVE PAD?

The FDA 510(k) record lists Delta Medical Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EVEN-TEMP. CAPACITIVE ADHESIVE PAD?

The FDA product code for EVEN-TEMP. CAPACITIVE ADHESIVE PAD is GEI.

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.

Other records listing Delta Medical Electronics, 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.

Related Devices (Code: GEI)

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.

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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