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FDA 510(k)

TROCAR CATHETER

K-Number: K851979 · 1985-06-17

ApplicantHospital Products Group
Decision Date1985-06-17
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TROCAR CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Hospital Products Group. It received FDA 510(k) clearance on 1985-06-17 under 510(k) number K851979. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROCAR CATHETER?

TROCAR CATHETER is a medical device that received FDA 510(k) clearance on 1985-06-17. The listed applicant is Hospital Products Group. The 510(k) number is K851979.

When did TROCAR CATHETER receive FDA 510(k) clearance?

TROCAR CATHETER received FDA 510(k) clearance on 1985-06-17, under 510(k) number K851979.

Who is the listed applicant for TROCAR CATHETER?

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

What is the FDA product code for TROCAR CATHETER?

The FDA product code for TROCAR CATHETER is JOL.

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Related Devices (Code: JOL)

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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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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