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FDA 510(k)

STRETCH WRAP

K-Number: K915446 · 1992-05-06

ApplicantSun Glitz Corp.
Decision Date1992-05-06
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRETCH WRAP is the device name listed in this FDA 510(k) record. The listed applicant is Sun Glitz Corp.. It received FDA 510(k) clearance on 1992-05-06 under 510(k) number K915446. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRETCH WRAP?

STRETCH WRAP is a medical device that received FDA 510(k) clearance on 1992-05-06. The listed applicant is Sun Glitz Corp.. The 510(k) number is K915446.

When did STRETCH WRAP receive FDA 510(k) clearance?

STRETCH WRAP received FDA 510(k) clearance on 1992-05-06, under 510(k) number K915446.

Who is the listed applicant for STRETCH WRAP?

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

What is the FDA product code for STRETCH WRAP?

The FDA product code for STRETCH WRAP is KGX.

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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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