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FDA 510(k)

VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE

K-Number: K943521 · 1995-02-14

ApplicantSchiff & Co.
Decision Date1995-02-14
Product CodeFRA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE is the device name listed in this FDA 510(k) record. The listed applicant is Schiff & Co.. It received FDA 510(k) clearance on 1995-02-14 under 510(k) number K943521. The device is classified under product code FRA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE?

VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE is a medical device that received FDA 510(k) clearance on 1995-02-14. The listed applicant is Schiff & Co.. The 510(k) number is K943521.

When did VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE receive FDA 510(k) clearance?

VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE received FDA 510(k) clearance on 1995-02-14, under 510(k) number K943521.

Who is the listed applicant for VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE?

The FDA 510(k) record lists Schiff & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE?

The FDA product code for VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE is FRA.

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Other records listing Schiff & Co. as applicant

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Related Devices (Code: FRA)

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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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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