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FDA 510(k)

VARIANT OF OCTOSTOP AND OCTOPAQUE

K-Number: K930124 · 1994-02-09

ApplicantOctostop, Inc.
Decision Date1994-02-09
Product CodeKXH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIANT OF OCTOSTOP AND OCTOPAQUE is the device name listed in this FDA 510(k) record. The listed applicant is Octostop, Inc.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K930124. The device is classified under product code KXH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIANT OF OCTOSTOP AND OCTOPAQUE?

VARIANT OF OCTOSTOP AND OCTOPAQUE is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Octostop, Inc.. The 510(k) number is K930124.

When did VARIANT OF OCTOSTOP AND OCTOPAQUE receive FDA 510(k) clearance?

VARIANT OF OCTOSTOP AND OCTOPAQUE received FDA 510(k) clearance on 1994-02-09, under 510(k) number K930124.

Who is the listed applicant for VARIANT OF OCTOSTOP AND OCTOPAQUE?

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

What is the FDA product code for VARIANT OF OCTOSTOP AND OCTOPAQUE?

The FDA product code for VARIANT OF OCTOSTOP AND OCTOPAQUE is KXH.

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Other records listing Octostop, 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.

K972766PIVOTING COMPENSATING FILTERS FOR THE HEADK963941THE PHARAOH COMPENSATING FILTERK953246OCTOROLLK952871RIDGES PLUSK942916OCTOPAQUE UNIVERSALK940306OCTOSTOP COMPENSATING FILTERS

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Related Devices (Code: KXH)

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.

K122174PEDIATRIC POSITIONER PAD SETGe Healthcare Coils (Usa Instruments, Inc.)K953246OCTOROLLOctostop, Inc.K933134SPECTRUM DG-P7000 PEDIATRIC CRADLESpectrum X-Ray Corp.K930357ACCESSORY TO UNIVERSAL OCTOPAQUEOctostop, Inc.K884292STRETCHER TABLEFischer Imaging Corp.K863890MAMM-AIREAr Custom Medical Products, Ltd.

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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