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FDA 510(k)

BLOOD SAFETY MODULE BSM2

K-Number: K833440 · 1983-12-08

Decision Date1983-12-08
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BLOOD SAFETY MODULE BSM2 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 1983-12-08 under 510(k) number K833440. 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 BLOOD SAFETY MODULE BSM2?

BLOOD SAFETY MODULE BSM2 is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Hospal Medical Corp.. The 510(k) number is K833440.

When did BLOOD SAFETY MODULE BSM2 receive FDA 510(k) clearance?

BLOOD SAFETY MODULE BSM2 received FDA 510(k) clearance on 1983-12-08, under 510(k) number K833440.

Who is the listed applicant for BLOOD SAFETY MODULE BSM2?

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 BLOOD SAFETY MODULE BSM2?

The FDA product code for BLOOD SAFETY MODULE BSM2 is KOC.

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.

Other records listing Hospal Medical 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.

View all 55 devices →

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.

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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