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FDA 510(k)

HAWK ANAESTHESIA INDUCTION UNIT

K-Number: K981845 · 1998-11-03

Decision Date1998-11-03
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HAWK ANAESTHESIA INDUCTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Industrial Equipment. It received FDA 510(k) clearance on 1998-11-03 under 510(k) number K981845. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAWK ANAESTHESIA INDUCTION UNIT?

HAWK ANAESTHESIA INDUCTION UNIT is a medical device that received FDA 510(k) clearance on 1998-11-03. The listed applicant is Medical Industrial Equipment. The 510(k) number is K981845.

When did HAWK ANAESTHESIA INDUCTION UNIT receive FDA 510(k) clearance?

HAWK ANAESTHESIA INDUCTION UNIT received FDA 510(k) clearance on 1998-11-03, under 510(k) number K981845.

Who is the listed applicant for HAWK ANAESTHESIA INDUCTION UNIT?

The FDA 510(k) record lists Medical Industrial Equipment as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAWK ANAESTHESIA INDUCTION UNIT?

The FDA product code for HAWK ANAESTHESIA INDUCTION UNIT is BSZ.

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 Medical Industrial Equipment 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.

Related Devices (Code: BSZ)

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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