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FDA 510(k)

RADIONICS SIPHON LIMITING DEVICE (SLD)

K-Number: K962990 · 1996-10-23

ApplicantRadionics, Inc.
Decision Date1996-10-23
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RADIONICS SIPHON LIMITING DEVICE (SLD) is the device name listed in this FDA 510(k) record. The listed applicant is Radionics, Inc.. It received FDA 510(k) clearance on 1996-10-23 under 510(k) number K962990. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIONICS SIPHON LIMITING DEVICE (SLD)?

RADIONICS SIPHON LIMITING DEVICE (SLD) is a medical device that received FDA 510(k) clearance on 1996-10-23. The listed applicant is Radionics, Inc.. The 510(k) number is K962990.

When did RADIONICS SIPHON LIMITING DEVICE (SLD) receive FDA 510(k) clearance?

RADIONICS SIPHON LIMITING DEVICE (SLD) received FDA 510(k) clearance on 1996-10-23, under 510(k) number K962990.

Who is the listed applicant for RADIONICS SIPHON LIMITING DEVICE (SLD)?

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

What is the FDA product code for RADIONICS SIPHON LIMITING DEVICE (SLD)?

The FDA product code for RADIONICS SIPHON LIMITING DEVICE (SLD) is JXG.

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Other records listing Radionics, Inc. as applicant

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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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