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FDA 510(k)

BIOPSY NEEDLES VARIOUS

K-Number: K840401 · 1984-03-12

ApplicantE-Z-Em, Inc.
Decision Date1984-03-12
Product Code
DecisionSubstantially Equivalent

Device Summary

BIOPSY NEEDLES VARIOUS is the device name listed in this FDA 510(k) record. The listed applicant is E-Z-Em, Inc.. It received FDA 510(k) clearance on 1984-03-12 under 510(k) number K840401. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPSY NEEDLES VARIOUS?

BIOPSY NEEDLES VARIOUS is a medical device that received FDA 510(k) clearance on 1984-03-12. The listed applicant is E-Z-Em, Inc.. The 510(k) number is K840401.

When did BIOPSY NEEDLES VARIOUS receive FDA 510(k) clearance?

BIOPSY NEEDLES VARIOUS received FDA 510(k) clearance on 1984-03-12, under 510(k) number K840401.

Who is the listed applicant for BIOPSY NEEDLES VARIOUS?

The FDA 510(k) record lists E-Z-Em, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing E-Z-Em, Inc. 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.

K071378MODIFICATION TO EMPOWER CT/CTA INJECTOR SYSTEM, MODELS 9800/9900 PRODUCT SERIESK062449EMPOWERMR INJECTOR SYSTEM, MODEL 9730K063029EMPOWER CT/CTA INJECTOR SYSTEM, MODEL 9800/9900K053008E-Z-EM ENDOSCOPIC CO2 REGULATORK041178EMPOWER TRANSFER SET, (CAT. NO. 7725)K031571EMPOWERCTA INJECTOR SYSTEM, MODELS 9930 & 9910 & 9825

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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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