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FDA 510(k)

BSM 21 BLOOD SAFETY MODULE

K-Number: K852135 · 1985-06-12

Decision Date1985-06-12
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BSM 21 BLOOD SAFETY MODULE 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 1985-06-12 under 510(k) number K852135. 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 BSM 21 BLOOD SAFETY MODULE?

BSM 21 BLOOD SAFETY MODULE is a medical device that received FDA 510(k) clearance on 1985-06-12. The listed applicant is Hospal Medical Corp.. The 510(k) number is K852135.

When did BSM 21 BLOOD SAFETY MODULE receive FDA 510(k) clearance?

BSM 21 BLOOD SAFETY MODULE received FDA 510(k) clearance on 1985-06-12, under 510(k) number K852135.

Who is the listed applicant for BSM 21 BLOOD SAFETY MODULE?

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 BSM 21 BLOOD SAFETY MODULE?

The FDA product code for BSM 21 BLOOD SAFETY MODULE 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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