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FDA 510(k)

BONE MARROW COLLECTION KIT AND STAND

K-Number: K871198 · 1987-11-06

ApplicantBaxter Healthcare Corp
Decision Date1987-11-06
Product CodeLWE
DecisionSubstantially Equivalent

Device Summary

BONE MARROW COLLECTION KIT AND STAND is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1987-11-06 under 510(k) number K871198. The device is classified under product code LWE. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONE MARROW COLLECTION KIT AND STAND?

BONE MARROW COLLECTION KIT AND STAND is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K871198.

When did BONE MARROW COLLECTION KIT AND STAND receive FDA 510(k) clearance?

BONE MARROW COLLECTION KIT AND STAND received FDA 510(k) clearance on 1987-11-06, under 510(k) number K871198.

Who is the listed applicant for BONE MARROW COLLECTION KIT AND STAND?

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

What is the FDA product code for BONE MARROW COLLECTION KIT AND STAND?

The FDA product code for BONE MARROW COLLECTION KIT AND STAND is LWE.

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Other records listing Baxter Healthcare Corp as applicant

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Related Devices (Code: LWE)

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.

K952350JAMSHIDI STYLE BIOPSY NEEDLE (ACRI) (BIOMID), ILLINOIS STYLE BIOPSY NEEDLE (ISAN)Promedical , Ltd.K913306BONE-TEMNO/STERNUM-TEMNOProact, Ltd.

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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