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FDA 510(k)

ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE

K-Number: K843690 · 1984-10-25

ApplicantPopper & Sons, Inc.
Decision Date1984-10-25
Product CodeGDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE 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 1984-10-25 under 510(k) number K843690. The device is classified under product code GDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE?

ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 1984-10-25. The listed applicant is Popper & Sons, Inc.. The 510(k) number is K843690.

When did ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE receive FDA 510(k) clearance?

ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE received FDA 510(k) clearance on 1984-10-25, under 510(k) number K843690.

Who is the listed applicant for ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE?

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

What is the FDA product code for ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE?

The FDA product code for ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE is GDM.

Related Clinical Trials

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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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/ASPIK842406WESCOTT TYPE BIOPSY NEEDLEK841300ANTRUM NEEDLE-WOLF TYPEK841301GARDNER TYPE BONE MARROW NEEDLEK841299BIERMAN BIOPSY NEEDLE

View all 8 devices →

Related Devices (Code: GDM)

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.

K071732MARROWMINERStemcor Systems, Inc.K971114BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K953082ILIAC CREST BONE MARROW ASPIRATION NEEDLEBaxter Healthcare CorpK953064BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K936207ENDO-NEEDLE INSTRUMENTGerard Medical, Inc.K930160ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLESymbiosis Corp.

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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