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FDA 510(k)

FILTER, PERITONEAL DIALY. ADMIN. SET

K-Number: K772236 · 1978-01-24

ApplicantMillipore Corp.
Decision Date1978-01-24
Product CodeKDJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FILTER, PERITONEAL DIALY. ADMIN. SET is the device name listed in this FDA 510(k) record. The listed applicant is Millipore Corp.. It received FDA 510(k) clearance on 1978-01-24 under 510(k) number K772236. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILTER, PERITONEAL DIALY. ADMIN. SET?

FILTER, PERITONEAL DIALY. ADMIN. SET is a medical device that received FDA 510(k) clearance on 1978-01-24. The listed applicant is Millipore Corp.. The 510(k) number is K772236.

When did FILTER, PERITONEAL DIALY. ADMIN. SET receive FDA 510(k) clearance?

FILTER, PERITONEAL DIALY. ADMIN. SET received FDA 510(k) clearance on 1978-01-24, under 510(k) number K772236.

Who is the listed applicant for FILTER, PERITONEAL DIALY. ADMIN. SET?

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

What is the FDA product code for FILTER, PERITONEAL DIALY. ADMIN. SET?

The FDA product code for FILTER, PERITONEAL DIALY. ADMIN. SET is KDJ.

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Other records listing Millipore 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.

K023892MILLEX VV, GV, AND HV SYRINGE FILTER UNITSK013988MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 RK963717MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)K941326ULTRAFREE-CLK934069MILLEX, DUALEX (PLUS, ULTRA)K924347WATERS(TM) 996 PDA

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Related Devices (Code: KDJ)

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.

K250404stay•safe® catheter extension set with Safe- Lock, 12 inch; stay•safe® catheter extension set with Luer-Lock, 6 inch; stay•safe® catheter extension set with Luer-Lock, 12 inch; stay•safe® catheter extension set with Luer-Lock, 18 inch; stay•safe® to Luer-Lock Adapter, 4 inchFresenius Medical Care Renal Therapies Group, LLCK231849MiniCap Extended Life PD Transfer Set with Twist Clamp - Code 5C4482A; MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short - Code 5C4483Baxter HealthcareK21401615L Cycler Drainage BagBaxter Healthcare CorporationK192705MiniCap Extended Life PD Transfer SetsBaxter HealthcareK173593stay•safe catheter extension set with Safe-Lock, 12 inch, stay•safe catheter extension set with Luer-Lock, 6 inch, stay•safe catheter extension set with Luer-Lock, 12 inch, stay•safe catheter extension set with Luer-Lock, 18 inch, stay•safe to Luer-Lock adapter, 4 inchFresenius Medical Care Renal Therapies Group, LLCK173651Multiple Tubing Segment Set with stay safe PIN Connectors, stay safe Drain SetFresenius Medical Care Renal Therapies Group, LLC

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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