FDA 510(k)

TIP, RUBBER, PERFORATED

K-Number: K760274 · 1976-08-30

ApplicantV. Mueller O.V. Baxter Healthcare Corp.

Decision Date1976-08-30

Product CodeFAJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

TIP, RUBBER, PERFORATED is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1976-08-30 under 510(k) number K760274. The device is classified under product code FAJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIP, RUBBER, PERFORATED?

TIP, RUBBER, PERFORATED is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760274.

When did TIP, RUBBER, PERFORATED receive FDA 510(k) clearance?

TIP, RUBBER, PERFORATED received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760274.

Who is the listed applicant for TIP, RUBBER, PERFORATED?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TIP, RUBBER, PERFORATED?

The FDA product code for TIP, RUBBER, PERFORATED is FAJ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.