FDA 510(k)

DMS 3000

K-Number: K792252 · 1980-03-12

Decision Date1980-03-12

Product CodeFKQ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

DMS 3000 is the device name listed in this FDA 510(k) record. The listed applicant is Renal Care Corp.. It received FDA 510(k) clearance on 1980-03-12 under 510(k) number K792252. The device is classified under product code FKQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMS 3000?

DMS 3000 is a medical device that received FDA 510(k) clearance on 1980-03-12. The listed applicant is Renal Care Corp.. The 510(k) number is K792252.

When did DMS 3000 receive FDA 510(k) clearance?

DMS 3000 received FDA 510(k) clearance on 1980-03-12, under 510(k) number K792252.

Who is the listed applicant for DMS 3000?

The FDA 510(k) record lists Renal Care Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DMS 3000?

The FDA product code for DMS 3000 is FKQ.

Other records listing Renal Care Corp. 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.

K810074ACCUFLO 100

Related Devices (Code: FKQ)

K052764DIACAP ULTRA DIALYSIS FLUID FILTERB. Braun Medizintechnologie GmbH K893612TWO TANK DISSOLUTION MODULENational Medical Care, Medical Products Div., Inc.K874084MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDMNational Medical Care, Medical Products Div., Inc.K873421KAWASUMI A.V. FISTULA SETKawasumi Laboratories Co., Ltd.K870889ACID FUCHSIN SOLUTIONSD.R.G. Scientific Industries K861730ACTRIL FOR KIDNEY MACHINE DISINFECTANTRenal Systems, Inc.

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.