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FDA 510(k)

CURAY-FORM

K-Number: K895222 · 1989-10-24

ApplicantScientific Pharmaceuticals, Inc.
Decision Date1989-10-24
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CURAY-FORM 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 1989-10-24 under 510(k) number K895222. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURAY-FORM?

CURAY-FORM is a medical device that received FDA 510(k) clearance on 1989-10-24. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K895222.

When did CURAY-FORM receive FDA 510(k) clearance?

CURAY-FORM received FDA 510(k) clearance on 1989-10-24, under 510(k) number K895222.

Who is the listed applicant for CURAY-FORM?

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 CURAY-FORM?

The FDA product code for CURAY-FORM is EBI.

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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.

K051952EUGENONEK041886PROVISOK013555SCI-PHARM POST SECUREK001446LIGHT-CURED ORTHODONTIC BAND CEMENTK993324CARBOCEM ZINC POLYCARBOXYLATE CEMENTK982915SCI-PHARM DFV VARNISH

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Related Devices (Code: EBI)

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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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