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FDA 510(k)

HYPODERMIC SYRINGE PISTON

K-Number: K950133 · 1995-04-13

ApplicantIspg, Inc.
Decision Date1995-04-13
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYPODERMIC SYRINGE PISTON is the device name listed in this FDA 510(k) record. The listed applicant is Ispg, Inc.. It received FDA 510(k) clearance on 1995-04-13 under 510(k) number K950133. 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 HYPODERMIC SYRINGE PISTON?

HYPODERMIC SYRINGE PISTON is a medical device that received FDA 510(k) clearance on 1995-04-13. The listed applicant is Ispg, Inc.. The 510(k) number is K950133.

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

HYPODERMIC SYRINGE PISTON received FDA 510(k) clearance on 1995-04-13, under 510(k) number K950133.

Who is the listed applicant for HYPODERMIC SYRINGE PISTON?

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

What is the FDA product code for HYPODERMIC SYRINGE PISTON?

The FDA product code for HYPODERMIC SYRINGE PISTON 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 Ispg, 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.

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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