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FDA 510(k)

GLASS SYRINGE

K-Number: K962042 · 1996-10-08

ApplicantIspg, Inc.
Decision Date1996-10-08
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GLASS SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Ispg, Inc.. It received FDA 510(k) clearance on 1996-10-08 under 510(k) number K962042. 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 GLASS SYRINGE?

GLASS SYRINGE is a medical device that received FDA 510(k) clearance on 1996-10-08. The listed applicant is Ispg, Inc.. The 510(k) number is K962042.

When did GLASS SYRINGE receive FDA 510(k) clearance?

GLASS SYRINGE received FDA 510(k) clearance on 1996-10-08, under 510(k) number K962042.

Who is the listed applicant for GLASS SYRINGE?

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 GLASS SYRINGE?

The FDA product code for GLASS SYRINGE 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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