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FDA 510(k)

BLOOD GROUPING SYS., BG-9

K-Number: K771098 · 1977-08-04

ApplicantTechnicon Instruments Corp.
Decision Date1977-08-04
Product CodeKSZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BLOOD GROUPING SYS., BG-9 is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K771098. The device is classified under product code KSZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD GROUPING SYS., BG-9?

BLOOD GROUPING SYS., BG-9 is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K771098.

When did BLOOD GROUPING SYS., BG-9 receive FDA 510(k) clearance?

BLOOD GROUPING SYS., BG-9 received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771098.

Who is the listed applicant for BLOOD GROUPING SYS., BG-9?

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

What is the FDA product code for BLOOD GROUPING SYS., BG-9?

The FDA product code for BLOOD GROUPING SYS., BG-9 is KSZ.

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Related Devices (Code: KSZ)

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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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