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FDA 510(k)

CERTODYN RAECG UNIVERSAL ADAPTER

K-Number: K973371 · 1997-11-24

Decision Date1997-11-24
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CERTODYN RAECG UNIVERSAL ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 1997-11-24 under 510(k) number K973371. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERTODYN RAECG UNIVERSAL ADAPTER?

CERTODYN RAECG UNIVERSAL ADAPTER is a medical device that received FDA 510(k) clearance on 1997-11-24. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K973371.

When did CERTODYN RAECG UNIVERSAL ADAPTER receive FDA 510(k) clearance?

CERTODYN RAECG UNIVERSAL ADAPTER received FDA 510(k) clearance on 1997-11-24, under 510(k) number K973371.

Who is the listed applicant for CERTODYN RAECG UNIVERSAL ADAPTER?

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

What is the FDA product code for CERTODYN RAECG UNIVERSAL ADAPTER?

The FDA product code for CERTODYN RAECG UNIVERSAL ADAPTER is DQY.

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 B.Braun Medical, 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 142 devices →

Related Devices (Code: DQY)

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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