FDA 510(k)

FIRST MEDIC MODEL 610P

K-Number: K895185 · 1989-10-27

Decision Date1989-10-27

Product CodeLDD

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

FIRST MEDIC MODEL 610P is the device name listed in this FDA 510(k) record. The listed applicant is First Medical Devices Corp.. It received FDA 510(k) clearance on 1989-10-27 under 510(k) number K895185. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRST MEDIC MODEL 610P?

FIRST MEDIC MODEL 610P is a medical device that received FDA 510(k) clearance on 1989-10-27. The listed applicant is First Medical Devices Corp.. The 510(k) number is K895185.

When did FIRST MEDIC MODEL 610P receive FDA 510(k) clearance?

FIRST MEDIC MODEL 610P received FDA 510(k) clearance on 1989-10-27, under 510(k) number K895185.

Who is the listed applicant for FIRST MEDIC MODEL 610P?

The FDA 510(k) record lists First Medical Devices Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIRST MEDIC MODEL 610P?

The FDA product code for FIRST MEDIC MODEL 610P is LDD.

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Other records listing First Medical Devices Corp. as applicant

K903657MODEL 610 MODIFIED K883584FIRST MEDIC MODE 610 K880780HEARTSTART 2000 DEFIBRILLATOR TESTER, ECG K871136HEARTSTART 2000, MANUAL DEFIBRILLATOR K871135HEARTSTART 2000, MANUAL MEDICAL CONTROL MODULE K860676HEARTSTART 2000

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Related Devices (Code: LDD)

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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.