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FDA 510(k)

MSI STERNUM ASPIRATION NEEDLE

K-Number: K820070 · 1982-02-04

ApplicantCreative Research and Mfg., Inc.
Decision Date1982-02-04
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MSI STERNUM ASPIRATION NEEDLE 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 1982-02-04 under 510(k) number K820070. 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 STERNUM ASPIRATION NEEDLE?

MSI STERNUM ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 1982-02-04. The listed applicant is Creative Research and Mfg., Inc.. The 510(k) number is K820070.

When did MSI STERNUM ASPIRATION NEEDLE receive FDA 510(k) clearance?

MSI STERNUM ASPIRATION NEEDLE received FDA 510(k) clearance on 1982-02-04, under 510(k) number K820070.

Who is the listed applicant for MSI STERNUM ASPIRATION NEEDLE?

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 STERNUM ASPIRATION NEEDLE?

The FDA product code for MSI STERNUM ASPIRATION NEEDLE 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.

K810248MSI BONE MARROW BIOPSY NEEDLE W/J TIP

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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