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FDA 510(k)

ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE

K-Number: K812685 · 1981-09-29

ApplicantEricka
Decision Date1981-09-29
Product CodeFJK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE is the device name listed in this FDA 510(k) record. The listed applicant is Ericka. It received FDA 510(k) clearance on 1981-09-29 under 510(k) number K812685. The device is classified under product code FJK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE?

ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE is a medical device that received FDA 510(k) clearance on 1981-09-29. The listed applicant is Ericka. The 510(k) number is K812685.

When did ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE receive FDA 510(k) clearance?

ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE received FDA 510(k) clearance on 1981-09-29, under 510(k) number K812685.

Who is the listed applicant for ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE?

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

What is the FDA product code for ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE?

The FDA product code for ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE is FJK.

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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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