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FDA 510(k)

CHILD SIZE - FILTER FLEX (TM)

K-Number: K893030 · 1989-09-18

ApplicantLife Design Systems, Inc.
Decision Date1989-09-18
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CHILD SIZE - FILTER FLEX (TM) 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 1989-09-18 under 510(k) number K893030. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHILD SIZE - FILTER FLEX (TM)?

CHILD SIZE - FILTER FLEX (TM) is a medical device that received FDA 510(k) clearance on 1989-09-18. The listed applicant is Life Design Systems, Inc.. The 510(k) number is K893030.

When did CHILD SIZE - FILTER FLEX (TM) receive FDA 510(k) clearance?

CHILD SIZE - FILTER FLEX (TM) received FDA 510(k) clearance on 1989-09-18, under 510(k) number K893030.

Who is the listed applicant for CHILD SIZE - FILTER FLEX (TM)?

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 CHILD SIZE - FILTER FLEX (TM)?

The FDA product code for CHILD SIZE - FILTER FLEX (TM) is CAH.

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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 TMK892862FLEX-CUP PERCUSSORK892221PULMONARY RESUSCITATOR, MODIFICATIONK890011OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBINGK890108MODIFIED CUSHION-FLEX(TM)

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Related Devices (Code: CAH)

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

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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