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FDA 510(k)

TUBE, STERILE CONDUCTIVE CONNECTING

K-Number: K760202 · 1976-07-19

ApplicantIpco Corp.
Decision Date1976-07-19
Product CodeGAZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TUBE, STERILE CONDUCTIVE CONNECTING is the device name listed in this FDA 510(k) record. The listed applicant is Ipco Corp.. It received FDA 510(k) clearance on 1976-07-19 under 510(k) number K760202. The device is classified under product code GAZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBE, STERILE CONDUCTIVE CONNECTING?

TUBE, STERILE CONDUCTIVE CONNECTING is a medical device that received FDA 510(k) clearance on 1976-07-19. The listed applicant is Ipco Corp.. The 510(k) number is K760202.

When did TUBE, STERILE CONDUCTIVE CONNECTING receive FDA 510(k) clearance?

TUBE, STERILE CONDUCTIVE CONNECTING received FDA 510(k) clearance on 1976-07-19, under 510(k) number K760202.

Who is the listed applicant for TUBE, STERILE CONDUCTIVE CONNECTING?

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

What is the FDA product code for TUBE, STERILE CONDUCTIVE CONNECTING?

The FDA product code for TUBE, STERILE CONDUCTIVE CONNECTING is GAZ.

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.

Other records listing Ipco 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.

View all 23 devices →

Related Devices (Code: GAZ)

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.

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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