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FDA 510(k)

SANAPLAST

K-Number: K881397 · 1988-06-14

ApplicantNebo Industries
Decision Date1988-06-14
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SANAPLAST is the device name listed in this FDA 510(k) record. The listed applicant is Nebo Industries. It received FDA 510(k) clearance on 1988-06-14 under 510(k) number K881397. 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 SANAPLAST?

SANAPLAST is a medical device that received FDA 510(k) clearance on 1988-06-14. The listed applicant is Nebo Industries. The 510(k) number is K881397.

When did SANAPLAST receive FDA 510(k) clearance?

SANAPLAST received FDA 510(k) clearance on 1988-06-14, under 510(k) number K881397.

Who is the listed applicant for SANAPLAST?

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

What is the FDA product code for SANAPLAST?

The FDA product code for SANAPLAST is KGX.

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Related Devices (Code: KGX)

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

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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