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FDA 510(k)

ISOTECHNOLOGIES LIFTSTATION & LIFTWORKS SOFTWARE

K-Number: K912175 · 1991-06-07

Decision Date1991-06-07
Product CodeINK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ISOTECHNOLOGIES LIFTSTATION & LIFTWORKS SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Isotechnologies, Inc.. It received FDA 510(k) clearance on 1991-06-07 under 510(k) number K912175. The device is classified under product code INK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISOTECHNOLOGIES LIFTSTATION & LIFTWORKS SOFTWARE?

ISOTECHNOLOGIES LIFTSTATION & LIFTWORKS SOFTWARE is a medical device that received FDA 510(k) clearance on 1991-06-07. The listed applicant is Isotechnologies, Inc.. The 510(k) number is K912175.

When did ISOTECHNOLOGIES LIFTSTATION & LIFTWORKS SOFTWARE receive FDA 510(k) clearance?

ISOTECHNOLOGIES LIFTSTATION & LIFTWORKS SOFTWARE received FDA 510(k) clearance on 1991-06-07, under 510(k) number K912175.

Who is the listed applicant for ISOTECHNOLOGIES LIFTSTATION & LIFTWORKS SOFTWARE?

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

What is the FDA product code for ISOTECHNOLOGIES LIFTSTATION & LIFTWORKS SOFTWARE?

The FDA product code for ISOTECHNOLOGIES LIFTSTATION & LIFTWORKS SOFTWARE is INK.

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 Isotechnologies, 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: INK)

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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