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FDA 510(k)

ELECTRO-MESH WRAP

K-Number: K840396 · 1984-04-30

ApplicantWhiting & Davis Co.
Decision Date1984-04-30
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRO-MESH WRAP is the device name listed in this FDA 510(k) record. The listed applicant is Whiting & Davis Co.. It received FDA 510(k) clearance on 1984-04-30 under 510(k) number K840396. 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-MESH WRAP?

ELECTRO-MESH WRAP is a medical device that received FDA 510(k) clearance on 1984-04-30. The listed applicant is Whiting & Davis Co.. The 510(k) number is K840396.

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

ELECTRO-MESH WRAP received FDA 510(k) clearance on 1984-04-30, under 510(k) number K840396.

Who is the listed applicant for ELECTRO-MESH WRAP?

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

What is the FDA product code for ELECTRO-MESH WRAP?

The FDA product code for ELECTRO-MESH WRAP 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 Whiting & Davis Co. 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.

K840395ELECTRO-MESH GLOVE

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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