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FDA 510(k)

ANTRUM NEEDLE-WOLF TYPE

K-Number: K841300 · 1984-06-05

ApplicantPopper & Sons, Inc.
Decision Date1984-06-05
Product Code
DecisionSubstantially Equivalent

Device Summary

ANTRUM NEEDLE-WOLF TYPE is the device name listed in this FDA 510(k) record. The listed applicant is Popper & Sons, Inc.. It received FDA 510(k) clearance on 1984-06-05 under 510(k) number K841300. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTRUM NEEDLE-WOLF TYPE?

ANTRUM NEEDLE-WOLF TYPE is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is Popper & Sons, Inc.. The 510(k) number is K841300.

When did ANTRUM NEEDLE-WOLF TYPE receive FDA 510(k) clearance?

ANTRUM NEEDLE-WOLF TYPE received FDA 510(k) clearance on 1984-06-05, under 510(k) number K841300.

Who is the listed applicant for ANTRUM NEEDLE-WOLF TYPE?

The FDA 510(k) record lists Popper & Sons, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Popper & Sons, 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.

K911397HYPODERMIC NEEDLES, SINGLE LUMENK843830J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPIK843690ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLEK842406WESCOTT TYPE BIOPSY NEEDLEK841301GARDNER TYPE BONE MARROW NEEDLEK841299BIERMAN BIOPSY NEEDLE

View all 8 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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