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FDA 510(k)

LINDLEY II RESUSCITATOR

K-Number: K881689 · 1988-07-08

ApplicantLindley Resuscitator, Inc.
Decision Date1988-07-08
Product CodeBYT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LINDLEY II RESUSCITATOR is the device name listed in this FDA 510(k) record. The listed applicant is Lindley Resuscitator, Inc.. It received FDA 510(k) clearance on 1988-07-08 under 510(k) number K881689. The device is classified under product code BYT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINDLEY II RESUSCITATOR?

LINDLEY II RESUSCITATOR is a medical device that received FDA 510(k) clearance on 1988-07-08. The listed applicant is Lindley Resuscitator, Inc.. The 510(k) number is K881689.

When did LINDLEY II RESUSCITATOR receive FDA 510(k) clearance?

LINDLEY II RESUSCITATOR received FDA 510(k) clearance on 1988-07-08, under 510(k) number K881689.

Who is the listed applicant for LINDLEY II RESUSCITATOR?

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

What is the FDA product code for LINDLEY II RESUSCITATOR?

The FDA product code for LINDLEY II RESUSCITATOR is BYT.

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Related Devices (Code: BYT)

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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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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