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FDA 510(k)

I.V. STARR KIT

K-Number: K912161 · 1991-10-08

ApplicantMedical Device Inspection Co., Inc.
Decision Date1991-10-08
Product CodeLKB
DecisionSubstantially Equivalent

Device Summary

I.V. STARR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Inspection Co., Inc.. It received FDA 510(k) clearance on 1991-10-08 under 510(k) number K912161. The device is classified under product code LKB. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.V. STARR KIT?

I.V. STARR KIT is a medical device that received FDA 510(k) clearance on 1991-10-08. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K912161.

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

I.V. STARR KIT received FDA 510(k) clearance on 1991-10-08, under 510(k) number K912161.

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

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

What is the FDA product code for I.V. STARR KIT?

The FDA product code for I.V. STARR KIT is LKB.

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Other records listing Medical Device Inspection Co., Inc. as applicant

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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Related Devices (Code: LKB)

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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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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