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FDA 510(k)

SARNS INFANT VENOUS RESERVOIR MODEL #16387

K-Number: K883345 · 1988-09-28

Applicant3M Health Care, Sarns
Decision Date1988-09-28
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SARNS INFANT VENOUS RESERVOIR MODEL #16387 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 1988-09-28 under 510(k) number K883345. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SARNS INFANT VENOUS RESERVOIR MODEL #16387?

SARNS INFANT VENOUS RESERVOIR MODEL #16387 is a medical device that received FDA 510(k) clearance on 1988-09-28. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K883345.

When did SARNS INFANT VENOUS RESERVOIR MODEL #16387 receive FDA 510(k) clearance?

SARNS INFANT VENOUS RESERVOIR MODEL #16387 received FDA 510(k) clearance on 1988-09-28, under 510(k) number K883345.

Who is the listed applicant for SARNS INFANT VENOUS RESERVOIR MODEL #16387?

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 INFANT VENOUS RESERVOIR MODEL #16387?

The FDA product code for SARNS INFANT VENOUS RESERVOIR MODEL #16387 is DTN.

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Other records listing 3M Health Care, Sarns as applicant

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Related Devices (Code: DTN)

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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