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FDA 510(k)

ASPIRATION NEEDLE

K-Number: K780784 · 1978-08-14

ApplicantFerris Mfg. Corp.
Decision Date1978-08-14
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ASPIRATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Ferris Mfg. Corp.. It received FDA 510(k) clearance on 1978-08-14 under 510(k) number K780784. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASPIRATION NEEDLE?

ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K780784.

When did ASPIRATION NEEDLE receive FDA 510(k) clearance?

ASPIRATION NEEDLE received FDA 510(k) clearance on 1978-08-14, under 510(k) number K780784.

Who is the listed applicant for ASPIRATION NEEDLE?

The FDA 510(k) record lists Ferris Mfg. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASPIRATION NEEDLE?

The FDA product code for ASPIRATION NEEDLE is KKX.

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Other records listing Ferris Mfg. Corp. 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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