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FDA 510(k)

MOBILE MATIC AUTOMATIC DONOR SCALE

K-Number: K810617 · 1981-04-07

Decision Date1981-04-07
Product CodeKSQ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MOBILE MATIC AUTOMATIC DONOR SCALE 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 1981-04-07 under 510(k) number K810617. 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 MOBILE MATIC AUTOMATIC DONOR SCALE?

MOBILE MATIC AUTOMATIC DONOR SCALE is a medical device that received FDA 510(k) clearance on 1981-04-07. The listed applicant is Lifeline Instruments, Inc.. The 510(k) number is K810617.

When did MOBILE MATIC AUTOMATIC DONOR SCALE receive FDA 510(k) clearance?

MOBILE MATIC AUTOMATIC DONOR SCALE received FDA 510(k) clearance on 1981-04-07, under 510(k) number K810617.

Who is the listed applicant for MOBILE MATIC AUTOMATIC DONOR SCALE?

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 MOBILE MATIC AUTOMATIC DONOR SCALE?

The FDA product code for MOBILE MATIC AUTOMATIC DONOR SCALE 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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