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FDA 510(k)

QUINTREX 0516 PROG. PULSE GENERATOR SYS

K-Number: K802224 · 1980-09-12

ApplicantMedcor, Inc.
Decision Date1980-09-12
Product Code
DecisionUnknown

Device Summary

QUINTREX 0516 PROG. PULSE GENERATOR SYS is the device name listed in this FDA 510(k) record. The listed applicant is Medcor, Inc.. It received FDA 510(k) clearance on 1980-09-12 under 510(k) number K802224. FDA Decision: Unknown.

Frequently Asked Questions

What is the QUINTREX 0516 PROG. PULSE GENERATOR SYS?

QUINTREX 0516 PROG. PULSE GENERATOR SYS is a medical device that received FDA 510(k) clearance on 1980-09-12. The listed applicant is Medcor, Inc.. The 510(k) number is K802224.

When did QUINTREX 0516 PROG. PULSE GENERATOR SYS receive FDA 510(k) clearance?

QUINTREX 0516 PROG. PULSE GENERATOR SYS received FDA 510(k) clearance on 1980-09-12, under 510(k) number K802224.

Who is the listed applicant for QUINTREX 0516 PROG. PULSE GENERATOR SYS?

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

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Other records listing Medcor, 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.

K792609LITHICRON 0520 P-SYNCHRONEOUS PULSE GEN.K802223QUINTREX 0515 PROGRAMMABLE PULSE GEN.K791678LITHICRON II 0403 IMPLANTABLE PACEMAKERK791095LITHICRON MODEL 0401, PACEMAKERK780430LITHICRON F PROGRAMMABLE PULSE GENK771538LITHICRON MODEL 3-70C-B PULSE GENERATOR

View all 8 devices →

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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