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FDA 510(k)

NUVO BARRIER FILM

K-Number: K980117 · 1998-12-18

ApplicantBiomedical Development Co.
Decision Date1998-12-18
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NUVO BARRIER FILM is the device name listed in this FDA 510(k) record. The listed applicant is Biomedical Development Co.. It received FDA 510(k) clearance on 1998-12-18 under 510(k) number K980117. 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 NUVO BARRIER FILM?

NUVO BARRIER FILM is a medical device that received FDA 510(k) clearance on 1998-12-18. The listed applicant is Biomedical Development Co.. The 510(k) number is K980117.

When did NUVO BARRIER FILM receive FDA 510(k) clearance?

NUVO BARRIER FILM received FDA 510(k) clearance on 1998-12-18, under 510(k) number K980117.

Who is the listed applicant for NUVO BARRIER FILM?

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

What is the FDA product code for NUVO BARRIER FILM?

The FDA product code for NUVO BARRIER FILM 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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