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FDA 510(k)

30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES

K-Number: K894801 · 1989-09-19

ApplicantAdvance Medical Designs, Inc.
Decision Date1989-09-19
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Advance Medical Designs, Inc.. It received FDA 510(k) clearance on 1989-09-19 under 510(k) number K894801. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES?

30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES is a medical device that received FDA 510(k) clearance on 1989-09-19. The listed applicant is Advance Medical Designs, Inc.. The 510(k) number is K894801.

When did 30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES receive FDA 510(k) clearance?

30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES received FDA 510(k) clearance on 1989-09-19, under 510(k) number K894801.

Who is the listed applicant for 30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES?

The FDA 510(k) record lists Advance Medical Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES?

The FDA product code for 30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES is FMF.

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Other records listing Advance Medical Designs, Inc. as applicant

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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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