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FDA 510(k)

PREMET, METAL PRIMER

K-Number: K884391 · 1989-01-03

ApplicantScientific Pharmaceuticals, Inc.
Decision Date1989-01-03
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PREMET, METAL PRIMER 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 1989-01-03 under 510(k) number K884391. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREMET, METAL PRIMER?

PREMET, METAL PRIMER is a medical device that received FDA 510(k) clearance on 1989-01-03. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K884391.

When did PREMET, METAL PRIMER receive FDA 510(k) clearance?

PREMET, METAL PRIMER received FDA 510(k) clearance on 1989-01-03, under 510(k) number K884391.

Who is the listed applicant for PREMET, METAL PRIMER?

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 PREMET, METAL PRIMER?

The FDA product code for PREMET, METAL PRIMER is EBF.

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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.

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Related Devices (Code: EBF)

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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