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FDA 510(k)

LEE BONE MARROW NEEDLES

K-Number: K842106 · 1984-08-10

ApplicantSouthland Instruments, Inc.
Decision Date1984-08-10
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LEE BONE MARROW NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Southland Instruments, Inc.. It received FDA 510(k) clearance on 1984-08-10 under 510(k) number K842106. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEE BONE MARROW NEEDLES?

LEE BONE MARROW NEEDLES is a medical device that received FDA 510(k) clearance on 1984-08-10. The listed applicant is Southland Instruments, Inc.. The 510(k) number is K842106.

When did LEE BONE MARROW NEEDLES receive FDA 510(k) clearance?

LEE BONE MARROW NEEDLES received FDA 510(k) clearance on 1984-08-10, under 510(k) number K842106.

Who is the listed applicant for LEE BONE MARROW NEEDLES?

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

What is the FDA product code for LEE BONE MARROW NEEDLES?

The FDA product code for LEE BONE MARROW NEEDLES is GAA.

Related Clinical Trials

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Other records listing Southland Instruments, 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.

K852897LEE BONE MARROW BIOPSY/ASPIRATION TRAY

Related Devices (Code: GAA)

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.

K223625CapnoSpot™ Pneumothorax Decompression IndicatorPneumeric, Inc.K102274ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENTArvik Enterprises/ Mini Lap TechnologiesK011586IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGEDiametrics Medical, Inc.K994151PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESXimed/Prosure/InjectxK983200INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXXimed/Prosure/InjectxK974741MANAN ACCURA NEEDLEMedical Device Technologies, Inc.

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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