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FDA 510(k)

LIFETECH CASSETTE

K-Number: K960756 · 1997-08-29

ApplicantLifetech Systems, Inc.
Decision Date1997-08-29
Product CodeKPJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIFETECH CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Lifetech Systems, Inc.. It received FDA 510(k) clearance on 1997-08-29 under 510(k) number K960756. The device is classified under product code KPJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFETECH CASSETTE?

LIFETECH CASSETTE is a medical device that received FDA 510(k) clearance on 1997-08-29. The listed applicant is Lifetech Systems, Inc.. The 510(k) number is K960756.

When did LIFETECH CASSETTE receive FDA 510(k) clearance?

LIFETECH CASSETTE received FDA 510(k) clearance on 1997-08-29, under 510(k) number K960756.

Who is the listed applicant for LIFETECH CASSETTE?

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

What is the FDA product code for LIFETECH CASSETTE?

The FDA product code for LIFETECH CASSETTE is KPJ.

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Related Devices (Code: KPJ)

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.

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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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