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FDA 510(k)

TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE

K-Number: K893003 · 1989-07-14

ApplicantUnited Medical Systems, Inc.
Decision Date1989-07-14
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE is the device name listed in this FDA 510(k) record. The listed applicant is United Medical Systems, Inc.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K893003. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE?

TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is United Medical Systems, Inc.. The 510(k) number is K893003.

When did TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE receive FDA 510(k) clearance?

TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893003.

Who is the listed applicant for TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE?

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

What is the FDA product code for TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE?

The FDA product code for TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE is FOZ.

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Other records listing United Medical Systems, 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.

K072538PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPTERK032958PIEZOLITH 3000 LITHOTRIPTER, MODEL 3000K894949SQAK863645SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000

Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, Inc.

Official Source

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