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FDA 510(k)

MSI BONE MARROW BIOPSY NEEDLE W/J TIP

K-Number: K810248 · 1981-03-20

ApplicantCreative Research and Mfg., Inc.
Decision Date1981-03-20
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MSI BONE MARROW BIOPSY NEEDLE W/J TIP is the device name listed in this FDA 510(k) record. The listed applicant is Creative Research and Mfg., Inc.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K810248. 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 MSI BONE MARROW BIOPSY NEEDLE W/J TIP?

MSI BONE MARROW BIOPSY NEEDLE W/J TIP is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Creative Research and Mfg., Inc.. The 510(k) number is K810248.

When did MSI BONE MARROW BIOPSY NEEDLE W/J TIP receive FDA 510(k) clearance?

MSI BONE MARROW BIOPSY NEEDLE W/J TIP received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810248.

Who is the listed applicant for MSI BONE MARROW BIOPSY NEEDLE W/J TIP?

The FDA 510(k) record lists Creative Research and Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MSI BONE MARROW BIOPSY NEEDLE W/J TIP?

The FDA product code for MSI BONE MARROW BIOPSY NEEDLE W/J TIP 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 Creative Research and Mfg., 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.

K820070MSI STERNUM ASPIRATION NEEDLE

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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