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FDA 510(k)

RAC 2A MODULE HOUSING

K-Number: K973984 · 1998-01-16

Decision Date1998-01-16
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RAC 2A MODULE HOUSING is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Medical Systems, Inc.. It received FDA 510(k) clearance on 1998-01-16 under 510(k) number K973984. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAC 2A MODULE HOUSING?

RAC 2A MODULE HOUSING is a medical device that received FDA 510(k) clearance on 1998-01-16. The listed applicant is Marquette Medical Systems, Inc.. The 510(k) number is K973984.

When did RAC 2A MODULE HOUSING receive FDA 510(k) clearance?

RAC 2A MODULE HOUSING received FDA 510(k) clearance on 1998-01-16, under 510(k) number K973984.

Who is the listed applicant for RAC 2A MODULE HOUSING?

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

What is the FDA product code for RAC 2A MODULE HOUSING?

The FDA product code for RAC 2A MODULE HOUSING is CCK.

Related Clinical Trials

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.

Other records listing Marquette Medical Systems, Inc. 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.

View all 9 devices →

Related Devices (Code: CCK)

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.

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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