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FDA 510(k)

BOEHRINGER MANNHEIM ELECSYS PRESICONTROL CARDIAC

K-Number: K983492 · 1998-10-09

ApplicantBoehringer Mannheim Corp.
Decision Date1998-10-09
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BOEHRINGER MANNHEIM ELECSYS PRESICONTROL CARDIAC 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 1998-10-09 under 510(k) number K983492. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOEHRINGER MANNHEIM ELECSYS PRESICONTROL CARDIAC?

BOEHRINGER MANNHEIM ELECSYS PRESICONTROL CARDIAC is a medical device that received FDA 510(k) clearance on 1998-10-09. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K983492.

When did BOEHRINGER MANNHEIM ELECSYS PRESICONTROL CARDIAC receive FDA 510(k) clearance?

BOEHRINGER MANNHEIM ELECSYS PRESICONTROL CARDIAC received FDA 510(k) clearance on 1998-10-09, under 510(k) number K983492.

Who is the listed applicant for BOEHRINGER MANNHEIM ELECSYS PRESICONTROL CARDIAC?

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 BOEHRINGER MANNHEIM ELECSYS PRESICONTROL CARDIAC?

The FDA product code for BOEHRINGER MANNHEIM ELECSYS PRESICONTROL CARDIAC is JJY.

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Other records listing Boehringer Mannheim Corp. as applicant

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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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