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FDA 510(k)

LIFELINE IPPB SET-UP

K-Number: K810341 · 1981-03-17

ApplicantTodd Industries, Inc.
Decision Date1981-03-17
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFELINE IPPB SET-UP is the device name listed in this FDA 510(k) record. The listed applicant is Todd Industries, Inc.. It received FDA 510(k) clearance on 1981-03-17 under 510(k) number K810341. 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 LIFELINE IPPB SET-UP?

LIFELINE IPPB SET-UP is a medical device that received FDA 510(k) clearance on 1981-03-17. The listed applicant is Todd Industries, Inc.. The 510(k) number is K810341.

When did LIFELINE IPPB SET-UP receive FDA 510(k) clearance?

LIFELINE IPPB SET-UP received FDA 510(k) clearance on 1981-03-17, under 510(k) number K810341.

Who is the listed applicant for LIFELINE IPPB SET-UP?

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

What is the FDA product code for LIFELINE IPPB SET-UP?

The FDA product code for LIFELINE IPPB SET-UP is BZO.

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Other records listing Todd Industries, 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.

K810340ADULT MASKS & PEDIATRIC MASKSK810362CORRUGATED FLEX TUBINGK810339NOSECLIP #6118K810361CONNECTOR ADAPTERSK810342NASAL CANNULAK810344OXYGEN TUBING

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Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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