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FDA 510(k)

ONE WEEK BACKSTOP DENTAL ANTI-RETRACTION CHECK VALVE

K-Number: K982009 · 1998-06-25

ApplicantScitech Solutions, Inc.
Decision Date1998-06-25
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ONE WEEK BACKSTOP DENTAL ANTI-RETRACTION CHECK VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Scitech Solutions, Inc.. It received FDA 510(k) clearance on 1998-06-25 under 510(k) number K982009. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONE WEEK BACKSTOP DENTAL ANTI-RETRACTION CHECK VALVE?

ONE WEEK BACKSTOP DENTAL ANTI-RETRACTION CHECK VALVE is a medical device that received FDA 510(k) clearance on 1998-06-25. The listed applicant is Scitech Solutions, Inc.. The 510(k) number is K982009.

When did ONE WEEK BACKSTOP DENTAL ANTI-RETRACTION CHECK VALVE receive FDA 510(k) clearance?

ONE WEEK BACKSTOP DENTAL ANTI-RETRACTION CHECK VALVE received FDA 510(k) clearance on 1998-06-25, under 510(k) number K982009.

Who is the listed applicant for ONE WEEK BACKSTOP DENTAL ANTI-RETRACTION CHECK VALVE?

The FDA 510(k) record lists Scitech Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ONE WEEK BACKSTOP DENTAL ANTI-RETRACTION CHECK VALVE?

The FDA product code for ONE WEEK BACKSTOP DENTAL ANTI-RETRACTION CHECK VALVE is EIA.

Related Clinical Trials

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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Other records listing Scitech Solutions, 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.

K973996CLEARLINE PLUS, DENTAL WATERLINE FILTERK960556BACSTOP DENTAL ANTI-RETRACTION CHECK VALVEK930144THE SCITECH ONE-DAY FILTER

Related Devices (Code: EIA)

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.

K251544Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)Lakong Medical Devices Co., Ltd.K251626Midmark Dental Delivery SystemMidmark CorporationK251491K5 Cart, K5 Mount, K5 SwingOsstem Implant Company., Ltd. Chair BusinessK243130Integral Dental UnitGuangdong Yadeng Medical Apparatus Co., Ltd.,K242611Integral Dental UnitsMipont Medical Equipment Co., Ltd.K250473Dental Delivery System Series 5 and Dental Delivery System Series 5 PlusDci International, LLC

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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