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FDA 510(k)

S-610 SHUNT ADAPTOR SET

K-Number: K811851 · 1981-08-31

ApplicantDravon Medical, Inc.
Decision Date1981-08-31
Product CodeKNR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

S-610 SHUNT ADAPTOR SET is the device name listed in this FDA 510(k) record. The listed applicant is Dravon Medical, Inc.. It received FDA 510(k) clearance on 1981-08-31 under 510(k) number K811851. The device is classified under product code KNR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S-610 SHUNT ADAPTOR SET?

S-610 SHUNT ADAPTOR SET is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is Dravon Medical, Inc.. The 510(k) number is K811851.

When did S-610 SHUNT ADAPTOR SET receive FDA 510(k) clearance?

S-610 SHUNT ADAPTOR SET received FDA 510(k) clearance on 1981-08-31, under 510(k) number K811851.

Who is the listed applicant for S-610 SHUNT ADAPTOR SET?

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

What is the FDA product code for S-610 SHUNT ADAPTOR SET?

The FDA product code for S-610 SHUNT ADAPTOR SET is KNR.

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Other records listing Dravon 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.

K873455S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSISK860770AM-100 I/A AMPACK832739STEDIFLO INFUSION SETK831842DRAVON T CLAMPK812771PERITONEAL DIALYSIS DRAINAGEK812772PERITONEAL DIALYSIS CYCLER SET (8UNIT)

View all 16 devices →

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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