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FDA 510(k)

8810 PUMP-PUMP SINGLE NEEDLE DEVICE

K-Number: K873279 · 1987-10-23

ApplicantCd Medical, Inc.
Decision Date1987-10-23
Product CodeFIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

8810 PUMP-PUMP SINGLE NEEDLE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Cd Medical, Inc.. It received FDA 510(k) clearance on 1987-10-23 under 510(k) number K873279. The device is classified under product code FIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 8810 PUMP-PUMP SINGLE NEEDLE DEVICE?

8810 PUMP-PUMP SINGLE NEEDLE DEVICE is a medical device that received FDA 510(k) clearance on 1987-10-23. The listed applicant is Cd Medical, Inc.. The 510(k) number is K873279.

When did 8810 PUMP-PUMP SINGLE NEEDLE DEVICE receive FDA 510(k) clearance?

8810 PUMP-PUMP SINGLE NEEDLE DEVICE received FDA 510(k) clearance on 1987-10-23, under 510(k) number K873279.

Who is the listed applicant for 8810 PUMP-PUMP SINGLE NEEDLE DEVICE?

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

What is the FDA product code for 8810 PUMP-PUMP SINGLE NEEDLE DEVICE?

The FDA product code for 8810 PUMP-PUMP SINGLE NEEDLE DEVICE is FIF.

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Other records listing Cd Medical, Inc. 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.

K925654CD HOME DIALYSERVICE HEMODIALYSIS TRAYK910215DRAKE WILLOCK SYSTEM 1000 DIALYSATE DELIVERY SYSTK901520WURTZ CHOLEY CLIP (TM)K894106DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYSTK884353ULTRX(TM) 850 ARTIFICIAL KIDNEYK880459480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATE

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Related Devices (Code: FIF)

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.

K820173COBE SINGLE-NEEDLE CONTROLLER #18-756Cobe Laboratories, Inc.K802230BELLCO SINGLE NEEDLE DOUBLE HEAD PUMPCardio Med Supplies, Inc.K801967MEDCOMP FEMORAL VEIN CATHETERMedical Components, Inc.K792174MODEL DM 353 & DM-353-L SINGLE NEEDLEExtracorporeal Medical Specialities, Inc.K772147GW 35 GUIDE WIRESorensen Research

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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