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FDA 510(k)

UVATAN INDUS. UVATAN 900C, 900B/800 & 600C

K-Number: K853587 · 1985-10-01

ApplicantUvatan Industries , Ltd.
Decision Date1985-10-01
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UVATAN INDUS. UVATAN 900C, 900B/800 & 600C is the device name listed in this FDA 510(k) record. The listed applicant is Uvatan Industries , Ltd.. It received FDA 510(k) clearance on 1985-10-01 under 510(k) number K853587. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UVATAN INDUS. UVATAN 900C, 900B/800 & 600C?

UVATAN INDUS. UVATAN 900C, 900B/800 & 600C is a medical device that received FDA 510(k) clearance on 1985-10-01. The listed applicant is Uvatan Industries , Ltd.. The 510(k) number is K853587.

When did UVATAN INDUS. UVATAN 900C, 900B/800 & 600C receive FDA 510(k) clearance?

UVATAN INDUS. UVATAN 900C, 900B/800 & 600C received FDA 510(k) clearance on 1985-10-01, under 510(k) number K853587.

Who is the listed applicant for UVATAN INDUS. UVATAN 900C, 900B/800 & 600C?

The FDA 510(k) record lists Uvatan Industries , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UVATAN INDUS. UVATAN 900C, 900B/800 & 600C?

The FDA product code for UVATAN INDUS. UVATAN 900C, 900B/800 & 600C is FTC.

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Related Devices (Code: FTC)

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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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