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FDA 510(k)

SYRINGE, DISPOSABLE, GLASS & PLASTIC

K-Number: K760005 · 1976-08-23

Decision Date1976-08-23
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGE, DISPOSABLE, GLASS & PLASTIC is the device name listed in this FDA 510(k) record. The listed applicant is Stewart-Naumann Laboratories. It received FDA 510(k) clearance on 1976-08-23 under 510(k) number K760005. 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 SYRINGE, DISPOSABLE, GLASS & PLASTIC?

SYRINGE, DISPOSABLE, GLASS & PLASTIC is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is Stewart-Naumann Laboratories. The 510(k) number is K760005.

When did SYRINGE, DISPOSABLE, GLASS & PLASTIC receive FDA 510(k) clearance?

SYRINGE, DISPOSABLE, GLASS & PLASTIC received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760005.

Who is the listed applicant for SYRINGE, DISPOSABLE, GLASS & PLASTIC?

The FDA 510(k) record lists Stewart-Naumann Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYRINGE, DISPOSABLE, GLASS & PLASTIC?

The FDA product code for SYRINGE, DISPOSABLE, GLASS & PLASTIC 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 Stewart-Naumann Laboratories 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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