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FDA 510(k)

LEE BONE MARROW BIOPSY/ASPIRATION TRAY

K-Number: K852897 · 1985-08-21

ApplicantSouthland Instruments, Inc.
Decision Date1985-08-21
Product CodeGAA
Advisory CommitteeSU
DecisionUnknown

Device Summary

LEE BONE MARROW BIOPSY/ASPIRATION TRAY 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 1985-08-21 under 510(k) number K852897. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the LEE BONE MARROW BIOPSY/ASPIRATION TRAY?

LEE BONE MARROW BIOPSY/ASPIRATION TRAY is a medical device that received FDA 510(k) clearance on 1985-08-21. The listed applicant is Southland Instruments, Inc.. The 510(k) number is K852897.

When did LEE BONE MARROW BIOPSY/ASPIRATION TRAY receive FDA 510(k) clearance?

LEE BONE MARROW BIOPSY/ASPIRATION TRAY received FDA 510(k) clearance on 1985-08-21, under 510(k) number K852897.

Who is the listed applicant for LEE BONE MARROW BIOPSY/ASPIRATION TRAY?

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 BIOPSY/ASPIRATION TRAY?

The FDA product code for LEE BONE MARROW BIOPSY/ASPIRATION TRAY is GAA.

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 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.

K842106LEE BONE MARROW NEEDLES

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

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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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