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FDA 510(k)

TRACOR, CANNULA, BICEPTS BIPOLAR

K-Number: K790043 · 1979-02-08

ApplicantNeomed Corp.
Decision Date1979-02-08
Product CodeHIN
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TRACOR, CANNULA, BICEPTS BIPOLAR is the device name listed in this FDA 510(k) record. The listed applicant is Neomed Corp.. It received FDA 510(k) clearance on 1979-02-08 under 510(k) number K790043. The device is classified under product code HIN. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACOR, CANNULA, BICEPTS BIPOLAR?

TRACOR, CANNULA, BICEPTS BIPOLAR is a medical device that received FDA 510(k) clearance on 1979-02-08. The listed applicant is Neomed Corp.. The 510(k) number is K790043.

When did TRACOR, CANNULA, BICEPTS BIPOLAR receive FDA 510(k) clearance?

TRACOR, CANNULA, BICEPTS BIPOLAR received FDA 510(k) clearance on 1979-02-08, under 510(k) number K790043.

Who is the listed applicant for TRACOR, CANNULA, BICEPTS BIPOLAR?

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

What is the FDA product code for TRACOR, CANNULA, BICEPTS BIPOLAR?

The FDA product code for TRACOR, CANNULA, BICEPTS BIPOLAR is HIN.

Related Clinical Trials

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.

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Other records listing Neomed Corp. 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.

K781810ELECTROSURGICAL UNIT 3001-3009K780118ELECTRODE, DISPERSIVE, DISP. NEOPAD

Related Devices (Code: HIN)

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.

K130305LINA BIPOLAR LOOP; STANDARD SIZE, LARGE SIZE, EXTRA LARGE SIZELina Medical ApsK122983KSEA BIPOLAR ELECTRODEKARL STORZ Endoscopy-America, Inc.K122605PKS BILLGyrus Acmi, Inc.K113080TUBALGATORMectra Labs, Inc.K111751VERSAPOINT II BIPOLAR ELECTROSURGERY GENERATOR, VERSAPOINT II 44MM ANGLED LOOP ELECTRODE, VERSAPOINT II FOOTSWITCH, VERSETHICON, Inc.K111059GYRUS ACMIL BIPOLARLAPROSCOPIC LOOP (PKS BILL)Gyrus Acmi, 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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