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FDA 510(k)

SARNS VENOATRIAL CATHETER

K-Number: K875048 · 1988-02-18

Applicant3M Health Care, Sarns
Decision Date1988-02-18
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SARNS VENOATRIAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Sarns. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K875048. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SARNS VENOATRIAL CATHETER?

SARNS VENOATRIAL CATHETER is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K875048.

When did SARNS VENOATRIAL CATHETER receive FDA 510(k) clearance?

SARNS VENOATRIAL CATHETER received FDA 510(k) clearance on 1988-02-18, under 510(k) number K875048.

Who is the listed applicant for SARNS VENOATRIAL CATHETER?

The FDA 510(k) record lists 3M Health Care, Sarns as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SARNS VENOATRIAL CATHETER?

The FDA product code for SARNS VENOATRIAL CATHETER is DWF.

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Other records listing 3M Health Care, Sarns as applicant

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Related Devices (Code: DWF)

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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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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