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FDA 510(k)

ENDO-LOK L-40 ENDOCARDIAL PACING ELECT.

K-Number: K760714 · 1976-12-14

ApplicantCoratomic, Inc.
Decision Date1976-12-14
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ENDO-LOK L-40 ENDOCARDIAL PACING ELECT. is the device name listed in this FDA 510(k) record. The listed applicant is Coratomic, Inc.. It received FDA 510(k) clearance on 1976-12-14 under 510(k) number K760714. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO-LOK L-40 ENDOCARDIAL PACING ELECT.?

ENDO-LOK L-40 ENDOCARDIAL PACING ELECT. is a medical device that received FDA 510(k) clearance on 1976-12-14. The listed applicant is Coratomic, Inc.. The 510(k) number is K760714.

When did ENDO-LOK L-40 ENDOCARDIAL PACING ELECT. receive FDA 510(k) clearance?

ENDO-LOK L-40 ENDOCARDIAL PACING ELECT. received FDA 510(k) clearance on 1976-12-14, under 510(k) number K760714.

Who is the listed applicant for ENDO-LOK L-40 ENDOCARDIAL PACING ELECT.?

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

What is the FDA product code for ENDO-LOK L-40 ENDOCARDIAL PACING ELECT.?

The FDA product code for ENDO-LOK L-40 ENDOCARDIAL PACING ELECT. is DTB.

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Other records listing Coratomic, 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.

K863365MODIFICATION OF STERILITY CYCLE PARAMETERSK822791CORATOMIC #VX5-105 & VX5-205 PULSE GEN.K820939C-101-PK821014CORATOMIC MODEL OVALITH 920BPK821033CORATOMIC MODEL OVALITH-920K810808CORATOMIC MODEL OVALITH-920

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Related Devices (Code: DTB)

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.

K061212BIOTRONIK ENDOCARDIAL PACING LEADSBiotronik, Inc.K041809PERMANENT PACING LEAD, MODEL PY2Oscor, Inc.K040569PERMANENT PACING LEAD, MODEL REFINO, MODEL: REFINO-R, RU, RJUOscor, Inc.K031274MODEL 5071 MYOCARDIAL PACING LEADMedtronic VascularK031210MODEL 4951M MYOCARDIAL UNIPOLAR LEADMetronic, Inc.K023205ELOX P 45-BP; ELOX P 53-BP; ELOX P 60-BPBiotronik, Inc.

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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