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FDA 510(k)

NOVADERM

K-Number: K896531 · 1990-04-13

ApplicantSyncare Corp.
Decision Date1990-04-13
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NOVADERM is the device name listed in this FDA 510(k) record. The listed applicant is Syncare Corp.. It received FDA 510(k) clearance on 1990-04-13 under 510(k) number K896531. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVADERM?

NOVADERM is a medical device that received FDA 510(k) clearance on 1990-04-13. The listed applicant is Syncare Corp.. The 510(k) number is K896531.

When did NOVADERM receive FDA 510(k) clearance?

NOVADERM received FDA 510(k) clearance on 1990-04-13, under 510(k) number K896531.

Who is the listed applicant for NOVADERM?

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

What is the FDA product code for NOVADERM?

The FDA product code for NOVADERM is KMF.

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Related Devices (Code: KMF)

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

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