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FDA 510(k)

CADD-TPN(TM) AMBULATORY INFUSION SYSTEM

K-Number: K931113 · 1994-04-28

ApplicantPharmacia Deltec, Inc.
Decision Date1994-04-28
Product CodeFIH
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CADD-TPN(TM) AMBULATORY INFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Deltec, Inc.. It received FDA 510(k) clearance on 1994-04-28 under 510(k) number K931113. The device is classified under product code FIH. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CADD-TPN(TM) AMBULATORY INFUSION SYSTEM?

CADD-TPN(TM) AMBULATORY INFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 1994-04-28. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K931113.

When did CADD-TPN(TM) AMBULATORY INFUSION SYSTEM receive FDA 510(k) clearance?

CADD-TPN(TM) AMBULATORY INFUSION SYSTEM received FDA 510(k) clearance on 1994-04-28, under 510(k) number K931113.

Who is the listed applicant for CADD-TPN(TM) AMBULATORY INFUSION SYSTEM?

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

What is the FDA product code for CADD-TPN(TM) AMBULATORY INFUSION SYSTEM?

The FDA product code for CADD-TPN(TM) AMBULATORY INFUSION SYSTEM is FIH.

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Other records listing Pharmacia Deltec, 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.

K943310MODEL 6100 AMBULATORY INFUSION SYSTEMK942046PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVEK942161LOCKBOXK942024PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEMK941445EXTENSION SET WITH ANTI-SIPHON VALVEK931073CATH-FINDER

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Related Devices (Code: FIH)

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.

K932055PERCUPUMP IIE-Z-Em, Inc.K935461VECTOR AMBULATORY DRUG DELIVERY SYSTEMInfusion Technology Intl.K900439SINGLE-USE, STERILE, PREFILLED SYRINGE, 60CCL H M Ent., Inc.K881707INTROCULAR FLUID INJECTORB&B Medical Assoc., 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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