SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT.
K-Number: K863824 · 1986-10-24
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Device Summary
Frequently Asked Questions
What is the SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT.?
SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT. is a medical device that received FDA 510(k) clearance on 1986-10-24. The listed applicant is D.R.G. Scientific Industries. The 510(k) number is K863824.
When did SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT. receive FDA 510(k) clearance?
SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT. received FDA 510(k) clearance on 1986-10-24, under 510(k) number K863824.
Who is the listed applicant for SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT.?
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 SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT.?
The FDA product code for SOLUTION/TEST STANDARD/CONDUCT. DIALY.&MULT.SOLUT. is FKH.
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.
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.
Related Devices (Code: FKH)
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.
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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