FDA 510(k)

KISS OF LIFE

K-Number: K891926 · 1989-08-21

Decision Date1989-08-21

Product CodeCAE

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

KISS OF LIFE is the device name listed in this FDA 510(k) record. The listed applicant is Anthony Don Michael, M.D.. It received FDA 510(k) clearance on 1989-08-21 under 510(k) number K891926. The device is classified under product code CAE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KISS OF LIFE?

KISS OF LIFE is a medical device that received FDA 510(k) clearance on 1989-08-21. The listed applicant is Anthony Don Michael, M.D.. The 510(k) number is K891926.

When did KISS OF LIFE receive FDA 510(k) clearance?

KISS OF LIFE received FDA 510(k) clearance on 1989-08-21, under 510(k) number K891926.

Who is the listed applicant for KISS OF LIFE?

The FDA 510(k) record lists Anthony Don Michael, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KISS OF LIFE?

The FDA product code for KISS OF LIFE is CAE.

Related Devices (Code: CAE)

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.

K033189KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT 303, KLT 304 AND KLT 305King Systems Corp.K033186KING LT-D DISPOSABLE OROPHARYNGEAL AIRWAY, MODELS KLT 203, KLT 204 AND KLT 205King Systems Corp.K021634KING LT, MODELS # KLT 100, KLT 101, KLT 102, KLT 103, KLT 104, KLT 105King Systems Corp.K955721CUFFED OROPHARYNGEAL AIRWAY (COPA)Mallinckrodt Medical K960240RUSCH OPTOSAFERusch Intl.K950613KEISEIKeisei (Usa) Co., Ltd.

Official Source

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