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FDA 510(k)

LIFECARE NASAL MASK KIT CAT. NO. 06-800

K-Number: K894779 · 1990-01-12

Decision Date1990-01-12
Product CodeBYE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFECARE NASAL MASK KIT CAT. NO. 06-800 is the device name listed in this FDA 510(k) record. The listed applicant is Lifecare Services, Inc.. It received FDA 510(k) clearance on 1990-01-12 under 510(k) number K894779. The device is classified under product code BYE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFECARE NASAL MASK KIT CAT. NO. 06-800?

LIFECARE NASAL MASK KIT CAT. NO. 06-800 is a medical device that received FDA 510(k) clearance on 1990-01-12. The listed applicant is Lifecare Services, Inc.. The 510(k) number is K894779.

When did LIFECARE NASAL MASK KIT CAT. NO. 06-800 receive FDA 510(k) clearance?

LIFECARE NASAL MASK KIT CAT. NO. 06-800 received FDA 510(k) clearance on 1990-01-12, under 510(k) number K894779.

Who is the listed applicant for LIFECARE NASAL MASK KIT CAT. NO. 06-800?

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

What is the FDA product code for LIFECARE NASAL MASK KIT CAT. NO. 06-800?

The FDA product code for LIFECARE NASAL MASK KIT CAT. NO. 06-800 is BYE.

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 Lifecare Services, 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.

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Related Devices (Code: BYE)

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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