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FDA 510(k)

CREATIVE CARE SYSTEMS' IV START KIT

K-Number: K863796 · 1986-11-28

ApplicantAmerican Biomaterials Corp.
Decision Date1986-11-28
Product CodeLRS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CREATIVE CARE SYSTEMS' IV START KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Biomaterials Corp.. It received FDA 510(k) clearance on 1986-11-28 under 510(k) number K863796. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CREATIVE CARE SYSTEMS' IV START KIT?

CREATIVE CARE SYSTEMS' IV START KIT is a medical device that received FDA 510(k) clearance on 1986-11-28. The listed applicant is American Biomaterials Corp.. The 510(k) number is K863796.

When did CREATIVE CARE SYSTEMS' IV START KIT receive FDA 510(k) clearance?

CREATIVE CARE SYSTEMS' IV START KIT received FDA 510(k) clearance on 1986-11-28, under 510(k) number K863796.

Who is the listed applicant for CREATIVE CARE SYSTEMS' IV START KIT?

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

What is the FDA product code for CREATIVE CARE SYSTEMS' IV START KIT?

The FDA product code for CREATIVE CARE SYSTEMS' IV START KIT is LRS.

Related Clinical Trials

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.

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Other records listing American Biomaterials 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.

K922455EVERT-O-CATH CATHETERK924725AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTSK915824HOLE PUNCHK880371BIOGLASS DENTAL ENDOSSEOUS RIDGE MAINTAINERK843461BIOGLASS OSSICULAR RECONSTRUCTION PROSTH

Related Devices (Code: LRS)

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.

K050654AMSINO I.V. START KITAmsino International, Inc.K001879INFUSION IV SETNirvi Intl. USAK963722IV START KITGrand Medical ProductsK951167EMS I.V. START KITEmergency Medical Supply, Inc.K950184B. BRAUN IV START KITSB. Braun of America, Inc.K944041PERSONAL HEARING SYSTEMResound Corp.

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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