Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

IV START KIT CUSTOM SMP # A-Z

K-Number: K922533 · 1993-03-23

Decision Date1993-03-23
Product CodeLRS
Advisory CommitteeHO
DecisionUnknown

Device Summary

IV START KIT CUSTOM SMP # A-Z is the device name listed in this FDA 510(k) record. The listed applicant is Specialty Medical Products Co.. It received FDA 510(k) clearance on 1993-03-23 under 510(k) number K922533. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the IV START KIT CUSTOM SMP # A-Z?

IV START KIT CUSTOM SMP # A-Z is a medical device that received FDA 510(k) clearance on 1993-03-23. The listed applicant is Specialty Medical Products Co.. The 510(k) number is K922533.

When did IV START KIT CUSTOM SMP # A-Z receive FDA 510(k) clearance?

IV START KIT CUSTOM SMP # A-Z received FDA 510(k) clearance on 1993-03-23, under 510(k) number K922533.

Who is the listed applicant for IV START KIT CUSTOM SMP # A-Z?

The FDA 510(k) record lists Specialty Medical Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IV START KIT CUSTOM SMP # A-Z?

The FDA product code for IV START KIT CUSTOM SMP # A-Z is LRS.

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.

Other records listing Specialty Medical Products Co. 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.

Related Devices (Code: LRS)

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.

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.

↑