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FDA 510(k)

SUNSOR ULTRAVIOLET METER

K-Number: K934728 · 1994-07-28

ApplicantSunsor, Inc.
Decision Date1994-07-28
Product CodeEAQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUNSOR ULTRAVIOLET METER is the device name listed in this FDA 510(k) record. The listed applicant is Sunsor, Inc.. It received FDA 510(k) clearance on 1994-07-28 under 510(k) number K934728. The device is classified under product code EAQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNSOR ULTRAVIOLET METER?

SUNSOR ULTRAVIOLET METER is a medical device that received FDA 510(k) clearance on 1994-07-28. The listed applicant is Sunsor, Inc.. The 510(k) number is K934728.

When did SUNSOR ULTRAVIOLET METER receive FDA 510(k) clearance?

SUNSOR ULTRAVIOLET METER received FDA 510(k) clearance on 1994-07-28, under 510(k) number K934728.

Who is the listed applicant for SUNSOR ULTRAVIOLET METER?

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

What is the FDA product code for SUNSOR ULTRAVIOLET METER?

The FDA product code for SUNSOR ULTRAVIOLET METER is EAQ.

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Related Devices (Code: EAQ)

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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