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FDA 510(k)

BONE MARROW ASPIRATION KIT

K-Number: K781371 · 1978-09-20

ApplicantFerris Mfg. Corp.
Decision Date1978-09-20
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BONE MARROW ASPIRATION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ferris Mfg. Corp.. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781371. 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 BONE MARROW ASPIRATION KIT?

BONE MARROW ASPIRATION KIT is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K781371.

When did BONE MARROW ASPIRATION KIT receive FDA 510(k) clearance?

BONE MARROW ASPIRATION KIT received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781371.

Who is the listed applicant for BONE MARROW ASPIRATION KIT?

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

What is the FDA product code for BONE MARROW ASPIRATION KIT?

The FDA product code for BONE MARROW ASPIRATION KIT is GAA.

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Other records listing Ferris Mfg. Corp. as applicant

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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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