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FDA 510(k)

KINDERWRAP

K-Number: K872003 · 1987-06-23

ApplicantThe Kinder Co.
Decision Date1987-06-23
Product CodeGAX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KINDERWRAP is the device name listed in this FDA 510(k) record. The listed applicant is The Kinder Co.. It received FDA 510(k) clearance on 1987-06-23 under 510(k) number K872003. The device is classified under product code GAX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINDERWRAP?

KINDERWRAP is a medical device that received FDA 510(k) clearance on 1987-06-23. The listed applicant is The Kinder Co.. The 510(k) number is K872003.

When did KINDERWRAP receive FDA 510(k) clearance?

KINDERWRAP received FDA 510(k) clearance on 1987-06-23, under 510(k) number K872003.

Who is the listed applicant for KINDERWRAP?

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

What is the FDA product code for KINDERWRAP?

The FDA product code for KINDERWRAP is GAX.

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Related Devices (Code: GAX)

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.

K931198UNIQUETIcat SystemsK881398TOURNIQUETBarretta Products, Research and Development, Inc.K881176STERILE ESMARCH BANDAGESpectrum/Hydro-Med Products, Inc.K875092DEGANIA SILICONE TOURNIQUETDegania Silicone , Ltd.K873928UNIVERSAL TOURNIQUETDryden Corp.K864897DALE VENIPUNCTURE TOURNIQUET, PRODUCT NO. 1335Dale Medical Products, Inc.

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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