FDA 510(k)

I.V. START KIT

K-Number: K851226 · 1985-05-01

Decision Date1985-05-01

Product Code

DecisionSubstantially Equivalent

Device Summary

I.V. START KIT is the device name listed in this FDA 510(k) record. The listed applicant is Perry, Div.. It received FDA 510(k) clearance on 1985-05-01 under 510(k) number K851226. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.V. START KIT?

I.V. START KIT is a medical device that received FDA 510(k) clearance on 1985-05-01. The listed applicant is Perry, Div.. The 510(k) number is K851226.

When did I.V. START KIT receive FDA 510(k) clearance?

I.V. START KIT received FDA 510(k) clearance on 1985-05-01, under 510(k) number K851226.

Who is the listed applicant for I.V. START KIT?

The FDA 510(k) record lists Perry, Div. as the applicant. This does not by itself establish the device manufacturer.

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.

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Other records listing Perry, Div. as applicant

K844610PERRY SUTURING SET W/ANESTHETIC K844609PERRY SUTURING SET K844001LANCE BLADES & SCALPELS K843125PERRY DERMAGUARD SURGICAL GLOVES K833920KELLY CHOLANGIOCATH

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.