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FDA 510(k)

LEE ASPIRATION NEEDLE

K-Number: K771574 · 1977-12-06

ApplicantRadiation Development Co., Inc.
Decision Date1977-12-06
Product CodeGDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LEE ASPIRATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Radiation Development Co., Inc.. It received FDA 510(k) clearance on 1977-12-06 under 510(k) number K771574. 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 LEE ASPIRATION NEEDLE?

LEE ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 1977-12-06. The listed applicant is Radiation Development Co., Inc.. The 510(k) number is K771574.

When did LEE ASPIRATION NEEDLE receive FDA 510(k) clearance?

LEE ASPIRATION NEEDLE received FDA 510(k) clearance on 1977-12-06, under 510(k) number K771574.

Who is the listed applicant for LEE ASPIRATION NEEDLE?

The FDA 510(k) record lists Radiation Development Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEE ASPIRATION NEEDLE?

The FDA product code for LEE 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.

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 Radiation Development Co., 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.

K772293BONE MARROW BIOPSY DEVICE

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

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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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