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FDA 510(k)

OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING

K-Number: K890011 · 1989-03-20

ApplicantLife Design Systems, Inc.
Decision Date1989-03-20
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Life Design Systems, Inc.. It received FDA 510(k) clearance on 1989-03-20 under 510(k) number K890011. 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 OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING?

OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING is a medical device that received FDA 510(k) clearance on 1989-03-20. The listed applicant is Life Design Systems, Inc.. The 510(k) number is K890011.

When did OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING receive FDA 510(k) clearance?

OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING received FDA 510(k) clearance on 1989-03-20, under 510(k) number K890011.

Who is the listed applicant for OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING?

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

What is the FDA product code for OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING?

The FDA product code for OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING is BZO.

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Other records listing Life Design Systems, 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.

K913714MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM)K885313HUMIDI-FLEX TMK893030CHILD SIZE - FILTER FLEX (TM)K892862FLEX-CUP PERCUSSORK892221PULMONARY RESUSCITATOR, MODIFICATIONK890108MODIFIED CUSHION-FLEX(TM)

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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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