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FDA 510(k)

HEATER WIRE BREATHING CIRCUIT

K-Number: K873179 · 1988-03-31

Decision Date1988-03-31
Product CodeBZE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HEATER WIRE BREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Life Design Systems, Inc.. It received FDA 510(k) clearance on 1988-03-31 under 510(k) number K873179. The device is classified under product code BZE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEATER WIRE BREATHING CIRCUIT?

HEATER WIRE BREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Life Design Systems, Inc.. The 510(k) number is K873179.

When did HEATER WIRE BREATHING CIRCUIT receive FDA 510(k) clearance?

HEATER WIRE BREATHING CIRCUIT received FDA 510(k) clearance on 1988-03-31, under 510(k) number K873179.

Who is the listed applicant for HEATER WIRE BREATHING CIRCUIT?

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

What is the FDA product code for HEATER WIRE BREATHING CIRCUIT?

The FDA product code for HEATER WIRE BREATHING CIRCUIT is BZE.

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 Life Design Systems, 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.

View all 29 devices →

Related Devices (Code: BZE)

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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