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FDA 510(k)

UNIVERSAL 2 S CENTRIFUGE

K-Number: K843087 · 1984-08-29

ApplicantBoehringer Mannheim Corp.
Decision Date1984-08-29
Product CodeJQC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL 2 S CENTRIFUGE 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 1984-08-29 under 510(k) number K843087. The device is classified under product code JQC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL 2 S CENTRIFUGE?

UNIVERSAL 2 S CENTRIFUGE is a medical device that received FDA 510(k) clearance on 1984-08-29. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K843087.

When did UNIVERSAL 2 S CENTRIFUGE receive FDA 510(k) clearance?

UNIVERSAL 2 S CENTRIFUGE received FDA 510(k) clearance on 1984-08-29, under 510(k) number K843087.

Who is the listed applicant for UNIVERSAL 2 S CENTRIFUGE?

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 UNIVERSAL 2 S CENTRIFUGE?

The FDA product code for UNIVERSAL 2 S CENTRIFUGE is JQC.

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Other records listing Boehringer Mannheim Corp. as applicant

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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Related Devices (Code: JQC)

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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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