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FDA 510(k)

FIRST RESPONSE EMERG. MEDICAL SYSTEM

K-Number: K841897 · 1984-07-23

ApplicantReed Products, Inc.
Decision Date1984-07-23
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FIRST RESPONSE EMERG. MEDICAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Reed Products, Inc.. It received FDA 510(k) clearance on 1984-07-23 under 510(k) number K841897. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRST RESPONSE EMERG. MEDICAL SYSTEM?

FIRST RESPONSE EMERG. MEDICAL SYSTEM is a medical device that received FDA 510(k) clearance on 1984-07-23. The listed applicant is Reed Products, Inc.. The 510(k) number is K841897.

When did FIRST RESPONSE EMERG. MEDICAL SYSTEM receive FDA 510(k) clearance?

FIRST RESPONSE EMERG. MEDICAL SYSTEM received FDA 510(k) clearance on 1984-07-23, under 510(k) number K841897.

Who is the listed applicant for FIRST RESPONSE EMERG. MEDICAL SYSTEM?

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

What is the FDA product code for FIRST RESPONSE EMERG. MEDICAL SYSTEM?

The FDA product code for FIRST RESPONSE EMERG. MEDICAL SYSTEM is KGX.

Related Clinical Trials

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Other records listing Reed Products, 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.

K841898FIRST RESPONSE EMERG. MEDICSL - BURNSK841899FIRST RESPONSE EMERG. MEDICAL SYS BONESK841900FIRST RESPONSE EMERG. EYE INJURIES

Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, Inc.

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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