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FDA 510(k)

MODIFIED INTENDED USE OF MONOJECT BONE MARROW NEED

K-Number: K883014 · 1988-07-28

ApplicantSherwood Medical Co.
Decision Date1988-07-28
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED INTENDED USE OF MONOJECT BONE MARROW NEED is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K883014. 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 MODIFIED INTENDED USE OF MONOJECT BONE MARROW NEED?

MODIFIED INTENDED USE OF MONOJECT BONE MARROW NEED is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Sherwood Medical Co.. The 510(k) number is K883014.

When did MODIFIED INTENDED USE OF MONOJECT BONE MARROW NEED receive FDA 510(k) clearance?

MODIFIED INTENDED USE OF MONOJECT BONE MARROW NEED received FDA 510(k) clearance on 1988-07-28, under 510(k) number K883014.

Who is the listed applicant for MODIFIED INTENDED USE OF MONOJECT BONE MARROW NEED?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED INTENDED USE OF MONOJECT BONE MARROW NEED?

The FDA product code for MODIFIED INTENDED USE OF MONOJECT BONE MARROW NEED is GAA.

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Other records listing Sherwood Medical Co. 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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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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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