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FDA 510(k)

DONORMATIC (BLOOD COLLECTION DEVICE)

K-Number: K760743 · 1976-12-06

Decision Date1976-12-06
Product CodeKSQ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

DONORMATIC (BLOOD COLLECTION DEVICE) is the device name listed in this FDA 510(k) record. The listed applicant is Lifeline Instruments, Inc.. It received FDA 510(k) clearance on 1976-12-06 under 510(k) number K760743. The device is classified under product code KSQ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DONORMATIC (BLOOD COLLECTION DEVICE)?

DONORMATIC (BLOOD COLLECTION DEVICE) is a medical device that received FDA 510(k) clearance on 1976-12-06. The listed applicant is Lifeline Instruments, Inc.. The 510(k) number is K760743.

When did DONORMATIC (BLOOD COLLECTION DEVICE) receive FDA 510(k) clearance?

DONORMATIC (BLOOD COLLECTION DEVICE) received FDA 510(k) clearance on 1976-12-06, under 510(k) number K760743.

Who is the listed applicant for DONORMATIC (BLOOD COLLECTION DEVICE)?

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

What is the FDA product code for DONORMATIC (BLOOD COLLECTION DEVICE)?

The FDA product code for DONORMATIC (BLOOD COLLECTION DEVICE) is KSQ.

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 Lifeline Instruments, Inc. 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.

Related Devices (Code: KSQ)

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

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

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