FDA 510(k)

INSPIRON NEONATAL VENTILATOR CIRCUIT

K-Number: K821064 · 1982-05-03

Decision Date1982-05-03

Product CodeBZO

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

INSPIRON NEONATAL VENTILATOR CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1982-05-03 under 510(k) number K821064. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSPIRON NEONATAL VENTILATOR CIRCUIT?

INSPIRON NEONATAL VENTILATOR CIRCUIT is a medical device that received FDA 510(k) clearance on 1982-05-03. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K821064.

When did INSPIRON NEONATAL VENTILATOR CIRCUIT receive FDA 510(k) clearance?

INSPIRON NEONATAL VENTILATOR CIRCUIT received FDA 510(k) clearance on 1982-05-03, under 510(k) number K821064.

Who is the listed applicant for INSPIRON NEONATAL VENTILATOR CIRCUIT?

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

What is the FDA product code for INSPIRON NEONATAL VENTILATOR CIRCUIT?

The FDA product code for INSPIRON NEONATAL VENTILATOR CIRCUIT is BZO.

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Related Devices (Code: BZO)

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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.