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FDA 510(k)

SCI-PHARM DFV VARNISH

K-Number: K982915 · 1999-02-12

Decision Date1999-02-12
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SCI-PHARM DFV VARNISH is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1999-02-12 under 510(k) number K982915. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCI-PHARM DFV VARNISH?

SCI-PHARM DFV VARNISH is a medical device that received FDA 510(k) clearance on 1999-02-12. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K982915.

When did SCI-PHARM DFV VARNISH receive FDA 510(k) clearance?

SCI-PHARM DFV VARNISH received FDA 510(k) clearance on 1999-02-12, under 510(k) number K982915.

Who is the listed applicant for SCI-PHARM DFV VARNISH?

The FDA 510(k) record lists Scientific Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCI-PHARM DFV VARNISH?

The FDA product code for SCI-PHARM DFV VARNISH is LBH.

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 Scientific Pharmaceuticals, Inc. 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 72 devices →

Related Devices (Code: LBH)

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

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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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