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FDA 510(k)

END TIDAL CO2 SAMPLING CIRCUIT

K-Number: K860659 · 1986-04-17

ApplicantLife Design Systems, Inc.
Decision Date1986-04-17
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

END TIDAL CO2 SAMPLING CIRCUIT 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 1986-04-17 under 510(k) number K860659. 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 END TIDAL CO2 SAMPLING CIRCUIT?

END TIDAL CO2 SAMPLING CIRCUIT is a medical device that received FDA 510(k) clearance on 1986-04-17. The listed applicant is Life Design Systems, Inc.. The 510(k) number is K860659.

When did END TIDAL CO2 SAMPLING CIRCUIT receive FDA 510(k) clearance?

END TIDAL CO2 SAMPLING CIRCUIT received FDA 510(k) clearance on 1986-04-17, under 510(k) number K860659.

Who is the listed applicant for END TIDAL CO2 SAMPLING CIRCUIT?

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 END TIDAL CO2 SAMPLING CIRCUIT?

The FDA product code for END TIDAL CO2 SAMPLING CIRCUIT 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, MODIFICATIONK890011OXYGEN CONNECTOR AND OXYGEN DELIVERY 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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