SOFT-WEDGE(TM) SYRINGE
K-Number: K900879 · 1990-05-10
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Device Summary
Frequently Asked Questions
What is the SOFT-WEDGE(TM) SYRINGE?
SOFT-WEDGE(TM) SYRINGE is a medical device that received FDA 510(k) clearance on 1990-05-10. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K900879.
When did SOFT-WEDGE(TM) SYRINGE receive FDA 510(k) clearance?
SOFT-WEDGE(TM) SYRINGE received FDA 510(k) clearance on 1990-05-10, under 510(k) number K900879.
Who is the listed applicant for SOFT-WEDGE(TM) SYRINGE?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOFT-WEDGE(TM) SYRINGE?
The FDA product code for SOFT-WEDGE(TM) SYRINGE is DYG.
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 Baxter Healthcare 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: DYG)
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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