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FDA 510(k)

L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT

K-Number: K850151 · 1985-07-19

ApplicantLife Products, Inc.
Decision Date1985-07-19
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Life Products, Inc.. It received FDA 510(k) clearance on 1985-07-19 under 510(k) number K850151. 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 L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT?

L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT is a medical device that received FDA 510(k) clearance on 1985-07-19. The listed applicant is Life Products, Inc.. The 510(k) number is K850151.

When did L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT receive FDA 510(k) clearance?

L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT received FDA 510(k) clearance on 1985-07-19, under 510(k) number K850151.

Who is the listed applicant for L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT?

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

What is the FDA product code for L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT?

The FDA product code for L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT is BZO.

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Other records listing Life Products, Inc. as applicant

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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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