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FDA 510(k)

THE SCITECH ONE-DAY FILTER

K-Number: K930144 · 1994-02-22

ApplicantScitech Solutions, Inc.
Decision Date1994-02-22
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE SCITECH ONE-DAY FILTER 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 1994-02-22 under 510(k) number K930144. 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 THE SCITECH ONE-DAY FILTER?

THE SCITECH ONE-DAY FILTER is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Scitech Solutions, Inc.. The 510(k) number is K930144.

When did THE SCITECH ONE-DAY FILTER receive FDA 510(k) clearance?

THE SCITECH ONE-DAY FILTER received FDA 510(k) clearance on 1994-02-22, under 510(k) number K930144.

Who is the listed applicant for THE SCITECH ONE-DAY FILTER?

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 THE SCITECH ONE-DAY FILTER?

The FDA product code for THE SCITECH ONE-DAY FILTER is EIA.

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Other records listing Scitech Solutions, Inc. as applicant

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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