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FDA 510(k)

DESERET EPIDURAL CATHETER

K-Number: K834472 · 1984-01-13

ApplicantParke-Davis Co.
Decision Date1984-01-13
Product Code
DecisionSubstantially Equivalent

Device Summary

DESERET EPIDURAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1984-01-13 under 510(k) number K834472. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DESERET EPIDURAL CATHETER?

DESERET EPIDURAL CATHETER is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Parke-Davis Co.. The 510(k) number is K834472.

When did DESERET EPIDURAL CATHETER receive FDA 510(k) clearance?

DESERET EPIDURAL CATHETER received FDA 510(k) clearance on 1984-01-13, under 510(k) number K834472.

Who is the listed applicant for DESERET EPIDURAL CATHETER?

The FDA 510(k) record lists Parke-Davis Co. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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Other records listing Parke-Davis 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.

K861725INTRACATH INTRAVENOUS CATHETER PLACEMENT UNITK862119DESERET FLO-THRU INJECTATE TEMPERATURE SENSORK855120ATI DISPOSABLE BIOLOGICAL TEST PACKK860570ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICEK860290VIAPIC CENTRAL LINE CATHETERK852192DISPOSABLE STEAM BIOLOGICAL TEST PACK

View all 47 devices →

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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