SYRINGE, DISPOSABLE, GLASS & PLASTIC
K-Number: K760005 · 1976-08-23
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Device Summary
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
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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