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FDA 510(k)

RESCUER

K-Number: K822727 · 1982-09-28

ApplicantArmstrong Ind., Inc.
Decision Date1982-09-28
Product CodeCAE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESCUER is the device name listed in this FDA 510(k) record. The listed applicant is Armstrong Ind., Inc.. It received FDA 510(k) clearance on 1982-09-28 under 510(k) number K822727. 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 RESCUER?

RESCUER is a medical device that received FDA 510(k) clearance on 1982-09-28. The listed applicant is Armstrong Ind., Inc.. The 510(k) number is K822727.

When did RESCUER receive FDA 510(k) clearance?

RESCUER received FDA 510(k) clearance on 1982-09-28, under 510(k) number K822727.

Who is the listed applicant for RESCUER?

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

What is the FDA product code for RESCUER?

The FDA product code for RESCUER is CAE.

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Other records listing Armstrong Ind., 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.

K852281SCHILLER EKG COMBI MSG-IM SCOPE & RECORDERK852181ELECTROCARDIOGRAPHK852282SCHILLER MINISCOPE MS-2 EKG SCOPEK851705LARYNGOSCOPE

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 MedicalK960240RUSCH 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.

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