Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI

K-Number: K843830 · 1984-10-26

ApplicantPopper & Sons, Inc.
Decision Date1984-10-26
Product CodeGDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI 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 1984-10-26 under 510(k) number K843830. 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 J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI?

J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI is a medical device that received FDA 510(k) clearance on 1984-10-26. The listed applicant is Popper & Sons, Inc.. The 510(k) number is K843830.

When did J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI receive FDA 510(k) clearance?

J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI received FDA 510(k) clearance on 1984-10-26, under 510(k) number K843830.

Who is the listed applicant for J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI?

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 J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI?

The FDA product code for J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 LUMENK843690ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLEK842406WESCOTT 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.

↑