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FDA 510(k)

ACID FUCHSIN SOLUTIONS

K-Number: K870889 · 1987-07-08

ApplicantD.R.G. Scientific Industries
Decision Date1987-07-08
Product CodeFKQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACID FUCHSIN SOLUTIONS is the device name listed in this FDA 510(k) record. The listed applicant is D.R.G. Scientific Industries. It received FDA 510(k) clearance on 1987-07-08 under 510(k) number K870889. 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 ACID FUCHSIN SOLUTIONS?

ACID FUCHSIN SOLUTIONS is a medical device that received FDA 510(k) clearance on 1987-07-08. The listed applicant is D.R.G. Scientific Industries. The 510(k) number is K870889.

When did ACID FUCHSIN SOLUTIONS receive FDA 510(k) clearance?

ACID FUCHSIN SOLUTIONS received FDA 510(k) clearance on 1987-07-08, under 510(k) number K870889.

Who is the listed applicant for ACID FUCHSIN SOLUTIONS?

The FDA 510(k) record lists D.R.G. Scientific Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACID FUCHSIN SOLUTIONS?

The FDA product code for ACID FUCHSIN SOLUTIONS is FKQ.

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.

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Other records listing D.R.G. Scientific Industries 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.

K892329OSMOMETER STANDARD SOLUTIONSK863880BLOOD GASES/ PO2, PCO2 AND BLOOD PH ANALYSIS PROD.K863825CO-OXIMETER SOLUTIONSK863824SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT.

Related Devices (Code: FKQ)

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.

K052764DIACAP ULTRA DIALYSIS FLUID FILTERB. Braun Medizintechnologie GmbHK893612TWO 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.K861730ACTRIL FOR KIDNEY MACHINE DISINFECTANTRenal Systems, Inc.K864635FOUR TANK DISSOLUTION MODULENational Medical Care, Medical Products Div., 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.

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