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FDA 510(k)

DRESSING CHANGE KIT

K-Number: K761192 · 1977-02-28

Decision Date1977-02-28
Product CodeJOK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DRESSING CHANGE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Superior Plastic Products Corp.. It received FDA 510(k) clearance on 1977-02-28 under 510(k) number K761192. The device is classified under product code JOK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRESSING CHANGE KIT?

DRESSING CHANGE KIT is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is Superior Plastic Products Corp.. The 510(k) number is K761192.

When did DRESSING CHANGE KIT receive FDA 510(k) clearance?

DRESSING CHANGE KIT received FDA 510(k) clearance on 1977-02-28, under 510(k) number K761192.

Who is the listed applicant for DRESSING CHANGE KIT?

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

What is the FDA product code for DRESSING CHANGE KIT?

The FDA product code for DRESSING CHANGE KIT is JOK.

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 Superior Plastic 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.

View all 15 devices →

Related Devices (Code: JOK)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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