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FDA 510(k)

FUN-UV SYSTEM PACK TEST

K-Number: K812290 · 1981-08-31

ApplicantBoehringer Mannheim Corp.
Decision Date1981-08-31
Product CodeCDQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FUN-UV SYSTEM PACK TEST is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1981-08-31 under 510(k) number K812290. The device is classified under product code CDQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUN-UV SYSTEM PACK TEST?

FUN-UV SYSTEM PACK TEST is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K812290.

When did FUN-UV SYSTEM PACK TEST receive FDA 510(k) clearance?

FUN-UV SYSTEM PACK TEST received FDA 510(k) clearance on 1981-08-31, under 510(k) number K812290.

Who is the listed applicant for FUN-UV SYSTEM PACK TEST?

The FDA 510(k) record lists Boehringer Mannheim Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FUN-UV SYSTEM PACK TEST?

The FDA product code for FUN-UV SYSTEM PACK TEST is CDQ.

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Other records listing Boehringer Mannheim Corp. as applicant

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Related Devices (Code: CDQ)

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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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