FDA 510(k)

MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD.

K-Number: K895244 · 1990-02-12

ApplicantNational Medical Care, Medical Products Div., Inc.

Decision Date1990-02-12

Product CodeKOC

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD. is the device name listed in this FDA 510(k) record. The listed applicant is National Medical Care, Medical Products Div., Inc.. It received FDA 510(k) clearance on 1990-02-12 under 510(k) number K895244. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD.?

MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD. is a medical device that received FDA 510(k) clearance on 1990-02-12. The listed applicant is National Medical Care, Medical Products Div., Inc.. The 510(k) number is K895244.

When did MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD. receive FDA 510(k) clearance?

MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD. received FDA 510(k) clearance on 1990-02-12, under 510(k) number K895244.

Who is the listed applicant for MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD.?

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

What is the FDA product code for MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD.?

The FDA product code for MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD. is KOC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.