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FDA 510(k)

PISTON SYRINGE WITH NEEDLE

K-Number: K883033 · 1988-10-31

Decision Date1988-10-31
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PISTON SYRINGE WITH NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Select Sources, Inc.. It received FDA 510(k) clearance on 1988-10-31 under 510(k) number K883033. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PISTON SYRINGE WITH NEEDLE?

PISTON SYRINGE WITH NEEDLE is a medical device that received FDA 510(k) clearance on 1988-10-31. The listed applicant is Select Sources, Inc.. The 510(k) number is K883033.

When did PISTON SYRINGE WITH NEEDLE receive FDA 510(k) clearance?

PISTON SYRINGE WITH NEEDLE received FDA 510(k) clearance on 1988-10-31, under 510(k) number K883033.

Who is the listed applicant for PISTON SYRINGE WITH NEEDLE?

The FDA 510(k) record lists Select Sources, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PISTON SYRINGE WITH NEEDLE?

The FDA product code for PISTON SYRINGE WITH NEEDLE is FMF.

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.

Other records listing Select Sources, 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.

View all 7 devices →

Related Devices (Code: FMF)

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.

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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