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FDA 510(k)

HOSPAL BLOOD LINES

K-Number: K823707 · 1983-01-05

ApplicantHospal Medical Corp.
Decision Date1983-01-05
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOSPAL BLOOD LINES is the device name listed in this FDA 510(k) record. The listed applicant is Hospal Medical Corp.. It received FDA 510(k) clearance on 1983-01-05 under 510(k) number K823707. 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 HOSPAL BLOOD LINES?

HOSPAL BLOOD LINES is a medical device that received FDA 510(k) clearance on 1983-01-05. The listed applicant is Hospal Medical Corp.. The 510(k) number is K823707.

When did HOSPAL BLOOD LINES receive FDA 510(k) clearance?

HOSPAL BLOOD LINES received FDA 510(k) clearance on 1983-01-05, under 510(k) number K823707.

Who is the listed applicant for HOSPAL BLOOD LINES?

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

What is the FDA product code for HOSPAL BLOOD LINES?

The FDA product code for HOSPAL BLOOD LINES is KOC.

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Related Devices (Code: KOC)

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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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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