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FDA 510(k)

TELE TRENS TM 10

K-Number: K960884 · 1997-09-12

ApplicantLife Sensing Instrument Company, Inc.
Decision Date1997-09-12
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TELE TRENS TM 10 is the device name listed in this FDA 510(k) record. The listed applicant is Life Sensing Instrument Company, Inc.. It received FDA 510(k) clearance on 1997-09-12 under 510(k) number K960884. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELE TRENS TM 10?

TELE TRENS TM 10 is a medical device that received FDA 510(k) clearance on 1997-09-12. The listed applicant is Life Sensing Instrument Company, Inc.. The 510(k) number is K960884.

When did TELE TRENS TM 10 receive FDA 510(k) clearance?

TELE TRENS TM 10 received FDA 510(k) clearance on 1997-09-12, under 510(k) number K960884.

Who is the listed applicant for TELE TRENS TM 10?

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

What is the FDA product code for TELE TRENS TM 10?

The FDA product code for TELE TRENS TM 10 is DSI.

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Other records listing Life Sensing Instrument Company, Inc. as applicant

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Related Devices (Code: DSI)

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

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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