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FDA 510(k)

CURAY ANTERIOR/POSTERIOR RESTORATIVE

K-Number: K823510 · 1982-12-28

ApplicantScientific Pharmaceuticals, Inc.
Decision Date1982-12-28
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CURAY ANTERIOR/POSTERIOR RESTORATIVE 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 1982-12-28 under 510(k) number K823510. 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 CURAY ANTERIOR/POSTERIOR RESTORATIVE?

CURAY ANTERIOR/POSTERIOR RESTORATIVE is a medical device that received FDA 510(k) clearance on 1982-12-28. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K823510.

When did CURAY ANTERIOR/POSTERIOR RESTORATIVE receive FDA 510(k) clearance?

CURAY ANTERIOR/POSTERIOR RESTORATIVE received FDA 510(k) clearance on 1982-12-28, under 510(k) number K823510.

Who is the listed applicant for CURAY ANTERIOR/POSTERIOR RESTORATIVE?

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 ANTERIOR/POSTERIOR RESTORATIVE?

The FDA product code for CURAY ANTERIOR/POSTERIOR RESTORATIVE 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.

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

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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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, Inc.

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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