AUTOMATIC TEFLON INJECTION SYRINGE
K-Number: K810284 · 1981-03-11
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Device Summary
Frequently Asked Questions
What is the AUTOMATIC TEFLON INJECTION SYRINGE?
AUTOMATIC TEFLON INJECTION SYRINGE is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is R. Wolf Medical Instruments Corp.. The 510(k) number is K810284.
When did AUTOMATIC TEFLON INJECTION SYRINGE receive FDA 510(k) clearance?
AUTOMATIC TEFLON INJECTION SYRINGE received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810284.
Who is the listed applicant for AUTOMATIC TEFLON INJECTION SYRINGE?
The FDA 510(k) record lists R. Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTOMATIC TEFLON INJECTION SYRINGE?
The FDA product code for AUTOMATIC TEFLON INJECTION SYRINGE is KCP.
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 R. Wolf Medical Instruments Corp. 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: KCP)
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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