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FDA 510(k)

AUTO SYRINGE MODEL AS-3A

K-Number: K761307 · 1977-01-06

ApplicantBaxter Healthcare Corp
Decision Date1977-01-06
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AUTO SYRINGE MODEL AS-3A is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1977-01-06 under 510(k) number K761307. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SYRINGE MODEL AS-3A?

AUTO SYRINGE MODEL AS-3A is a medical device that received FDA 510(k) clearance on 1977-01-06. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K761307.

When did AUTO SYRINGE MODEL AS-3A receive FDA 510(k) clearance?

AUTO SYRINGE MODEL AS-3A received FDA 510(k) clearance on 1977-01-06, under 510(k) number K761307.

Who is the listed applicant for AUTO SYRINGE MODEL AS-3A?

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 AUTO SYRINGE MODEL AS-3A?

The FDA product code for AUTO SYRINGE MODEL AS-3A is FRN.

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Related Devices (Code: FRN)

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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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