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FDA 510(k)

TENCKHOFF PERITONEAL DIALYSIS KIT

K-Number: K902203 · 1990-08-01

ApplicantAkcess Medical Products, Inc.
Decision Date1990-08-01
Product CodeFJG
Advisory CommitteeGU
DecisionUnknown

Device Summary

TENCKHOFF PERITONEAL DIALYSIS KIT is the device name listed in this FDA 510(k) record. The listed applicant is Akcess Medical Products, Inc.. It received FDA 510(k) clearance on 1990-08-01 under 510(k) number K902203. The device is classified under product code FJG. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the TENCKHOFF PERITONEAL DIALYSIS KIT?

TENCKHOFF PERITONEAL DIALYSIS KIT is a medical device that received FDA 510(k) clearance on 1990-08-01. The listed applicant is Akcess Medical Products, Inc.. The 510(k) number is K902203.

When did TENCKHOFF PERITONEAL DIALYSIS KIT receive FDA 510(k) clearance?

TENCKHOFF PERITONEAL DIALYSIS KIT received FDA 510(k) clearance on 1990-08-01, under 510(k) number K902203.

Who is the listed applicant for TENCKHOFF PERITONEAL DIALYSIS KIT?

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

What is the FDA product code for TENCKHOFF PERITONEAL DIALYSIS KIT?

The FDA product code for TENCKHOFF PERITONEAL DIALYSIS KIT is FJG.

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Other records listing Akcess Medical Products, Inc. as applicant

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Related Devices (Code: FJG)

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.

K933681GAMBRO LUNDIA PRO 100, 500, 600 DIALYZERSCobe Renal Care, Inc.K933680GAMBRO LUNDIA PRO 200 DIALYZERCobe Renal Care, Inc.K920693DEXTROLYTE II PERITONEAL DIALYSIS 48-3028-9National Medical Care, Medical Products Div., Inc.K915504GAMBRO LUNDIA ALPHA HEMODIALYZERSC.G.H. Medical, Inc.K901368HEMOSPAL KITS A1, A2D, AO, & A1DGambro-Hospal, Inc.K862840GAMBRO LUNDIA 10-1L, 1N, 1H, 3H, 4N, 4H, 5H, 6NGambro, 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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