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FDA 510(k)

EMERSON TRO/CATH TROCAR CATHETERS

K-Number: K853132 · 1986-01-08

ApplicantJ. H. Emerson Co.
Decision Date1986-01-08
Product CodeDRC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EMERSON TRO/CATH TROCAR CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is J. H. Emerson Co.. It received FDA 510(k) clearance on 1986-01-08 under 510(k) number K853132. The device is classified under product code DRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMERSON TRO/CATH TROCAR CATHETERS?

EMERSON TRO/CATH TROCAR CATHETERS is a medical device that received FDA 510(k) clearance on 1986-01-08. The listed applicant is J. H. Emerson Co.. The 510(k) number is K853132.

When did EMERSON TRO/CATH TROCAR CATHETERS receive FDA 510(k) clearance?

EMERSON TRO/CATH TROCAR CATHETERS received FDA 510(k) clearance on 1986-01-08, under 510(k) number K853132.

Who is the listed applicant for EMERSON TRO/CATH TROCAR CATHETERS?

The FDA 510(k) record lists J. H. Emerson Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMERSON TRO/CATH TROCAR CATHETERS?

The FDA product code for EMERSON TRO/CATH TROCAR CATHETERS is DRC.

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Other records listing J. H. Emerson Co. 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.

K002598EMERSON COUGH ASSIST MODEL CA-3000 W/AUTOMATIC TIMING AND MODEL CM-3000 W/MANUAL TIMINGK920910OXYGEN POWERED RESUSCITATOR FOR CPRK924174EMERSON IN-EXSUFFLATOR, MODELS 2-CM & 2-CAK902764EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARMK896721MODEL 7-AT TREATMENT CHAMBERK881808EMERSON CHEST RESPIRATOR, MODEL 33-CRE

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Related Devices (Code: DRC)

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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