SYRINGES(2-PARTS SINGLE USE)
K-Number: K822532 · 1982-09-17
Advertisement
Device Summary
Frequently Asked Questions
What is the SYRINGES(2-PARTS SINGLE USE)?
SYRINGES(2-PARTS SINGLE USE) is a medical device that received FDA 510(k) clearance on 1982-09-17. The listed applicant is Impex Laboratories. The 510(k) number is K822532.
When did SYRINGES(2-PARTS SINGLE USE) receive FDA 510(k) clearance?
SYRINGES(2-PARTS SINGLE USE) received FDA 510(k) clearance on 1982-09-17, under 510(k) number K822532.
Who is the listed applicant for SYRINGES(2-PARTS SINGLE USE)?
The FDA 510(k) record lists Impex Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYRINGES(2-PARTS SINGLE USE)?
The FDA product code for SYRINGES(2-PARTS SINGLE USE) 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 Impex 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.
Advertisement