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FDA 510(k)

BONE MARROW BIOPSY PROCEDURE TRAY

K-Number: K930158 · 1993-07-02

ApplicantSymbiosis Corp.
Decision Date1993-07-02
Product CodeGAA
Advisory CommitteeSU
DecisionUnknown

Device Summary

BONE MARROW BIOPSY PROCEDURE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K930158. 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 BONE MARROW BIOPSY PROCEDURE TRAY?

BONE MARROW BIOPSY PROCEDURE TRAY is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Symbiosis Corp.. The 510(k) number is K930158.

When did BONE MARROW BIOPSY PROCEDURE TRAY receive FDA 510(k) clearance?

BONE MARROW BIOPSY PROCEDURE TRAY received FDA 510(k) clearance on 1993-07-02, under 510(k) number K930158.

Who is the listed applicant for BONE MARROW BIOPSY PROCEDURE TRAY?

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 BONE MARROW BIOPSY PROCEDURE TRAY?

The FDA product code for BONE MARROW BIOPSY PROCEDURE TRAY is GAA.

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Other records listing Symbiosis Corp. as applicant

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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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