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FDA 510(k)

RISKONTROL SINGLE USE

K-Number: K923876 · 1993-04-05

ApplicantRiskontrol
Decision Date1993-04-05
Product CodeECB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RISKONTROL SINGLE USE is the device name listed in this FDA 510(k) record. The listed applicant is Riskontrol. It received FDA 510(k) clearance on 1993-04-05 under 510(k) number K923876. The device is classified under product code ECB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RISKONTROL SINGLE USE?

RISKONTROL SINGLE USE is a medical device that received FDA 510(k) clearance on 1993-04-05. The listed applicant is Riskontrol. The 510(k) number is K923876.

When did RISKONTROL SINGLE USE receive FDA 510(k) clearance?

RISKONTROL SINGLE USE received FDA 510(k) clearance on 1993-04-05, under 510(k) number K923876.

Who is the listed applicant for RISKONTROL SINGLE USE?

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

What is the FDA product code for RISKONTROL SINGLE USE?

The FDA product code for RISKONTROL SINGLE USE is ECB.

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Related Devices (Code: ECB)

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.

K942519UNI-SYRINGE, UNI-TIP AND ACCESS SYRINGE TIPSBull Frog Mfg. Co.K931772SURETIP SYRINGE TIP COVERWestern M/D, Inc.K931137DENTAL SYRINGE TIPA-Dec, Inc.K923285PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLESmith & Nephew, Inc.K920499SANI-TIPDw Industries, Inc.K911756POSTERIOR NASAL EPISTAXIS INSTRUMENTSRichard Wolf Medical Instruments Corp.

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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