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FDA 510(k)

FISSURE SEALER AND BONDING AGENT

K-Number: K790788 · 1979-07-06

ApplicantScientific Pharmaceuticals, Inc.
Decision Date1979-07-06
Product CodeEBC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FISSURE SEALER AND BONDING AGENT 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 1979-07-06 under 510(k) number K790788. The device is classified under product code EBC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FISSURE SEALER AND BONDING AGENT?

FISSURE SEALER AND BONDING AGENT is a medical device that received FDA 510(k) clearance on 1979-07-06. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K790788.

When did FISSURE SEALER AND BONDING AGENT receive FDA 510(k) clearance?

FISSURE SEALER AND BONDING AGENT received FDA 510(k) clearance on 1979-07-06, under 510(k) number K790788.

Who is the listed applicant for FISSURE SEALER AND BONDING AGENT?

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 FISSURE SEALER AND BONDING AGENT?

The FDA product code for FISSURE SEALER AND BONDING AGENT is EBC.

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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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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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