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FDA 510(k)

UNIREST PL, ANTE./POST. RESTORATIVE, PASTE/LIQUID

K-Number: K884351 · 1988-12-28

ApplicantScientific Pharmaceuticals, Inc.
Decision Date1988-12-28
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UNIREST PL, ANTE./POST. RESTORATIVE, PASTE/LIQUID 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 1988-12-28 under 510(k) number K884351. 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 UNIREST PL, ANTE./POST. RESTORATIVE, PASTE/LIQUID?

UNIREST PL, ANTE./POST. RESTORATIVE, PASTE/LIQUID is a medical device that received FDA 510(k) clearance on 1988-12-28. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K884351.

When did UNIREST PL, ANTE./POST. RESTORATIVE, PASTE/LIQUID receive FDA 510(k) clearance?

UNIREST PL, ANTE./POST. RESTORATIVE, PASTE/LIQUID received FDA 510(k) clearance on 1988-12-28, under 510(k) number K884351.

Who is the listed applicant for UNIREST PL, ANTE./POST. RESTORATIVE, PASTE/LIQUID?

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 UNIREST PL, ANTE./POST. RESTORATIVE, PASTE/LIQUID?

The FDA product code for UNIREST PL, ANTE./POST. RESTORATIVE, PASTE/LIQUID 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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