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FDA 510(k)

SYMBIOSIS BONE MARROW BIOPSY NEEDLE

K-Number: K925416 · 1993-02-23

ApplicantSymbiosis Corp.
Decision Date1993-02-23
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SYMBIOSIS BONE MARROW BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1993-02-23 under 510(k) number K925416. 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 SYMBIOSIS BONE MARROW BIOPSY NEEDLE?

SYMBIOSIS BONE MARROW BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1993-02-23. The listed applicant is Symbiosis Corp.. The 510(k) number is K925416.

When did SYMBIOSIS BONE MARROW BIOPSY NEEDLE receive FDA 510(k) clearance?

SYMBIOSIS BONE MARROW BIOPSY NEEDLE received FDA 510(k) clearance on 1993-02-23, under 510(k) number K925416.

Who is the listed applicant for SYMBIOSIS BONE MARROW BIOPSY NEEDLE?

The FDA 510(k) record lists Symbiosis Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYMBIOSIS BONE MARROW BIOPSY NEEDLE?

The FDA product code for SYMBIOSIS BONE MARROW BIOPSY NEEDLE is GAA.

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Other records listing Symbiosis Corp. 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.

K955119SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953453SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODESK952432SYMBIOSIS BIPOLAR FORCEPSK951387SYMBIOSIS BIPOLAR SCISSORSK950286SYMBIOSIS BIPOLAR SCISSORS

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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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