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FDA 510(k)

INSPIRON NEBULO BASIC EXTERNAL HEATER

K-Number: K880304 · 1988-03-04

Decision Date1988-03-04
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSPIRON NEBULO BASIC EXTERNAL HEATER is the device name listed in this FDA 510(k) record. The listed applicant is Intertech Resources, Inc.. It received FDA 510(k) clearance on 1988-03-04 under 510(k) number K880304. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSPIRON NEBULO BASIC EXTERNAL HEATER?

INSPIRON NEBULO BASIC EXTERNAL HEATER is a medical device that received FDA 510(k) clearance on 1988-03-04. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K880304.

When did INSPIRON NEBULO BASIC EXTERNAL HEATER receive FDA 510(k) clearance?

INSPIRON NEBULO BASIC EXTERNAL HEATER received FDA 510(k) clearance on 1988-03-04, under 510(k) number K880304.

Who is the listed applicant for INSPIRON NEBULO BASIC EXTERNAL HEATER?

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

What is the FDA product code for INSPIRON NEBULO BASIC EXTERNAL HEATER?

The FDA product code for INSPIRON NEBULO BASIC EXTERNAL HEATER is CAF.

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 Intertech Resources, 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: CAF)

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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