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FDA 510(k)

P-S MEDICAL CSF-SIPHON CONTROL DEVICE

K-Number: K862907 · 1986-12-03

ApplicantPudenz-Schulte Medical Research Corp.
Decision Date1986-12-03
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

P-S MEDICAL CSF-SIPHON CONTROL DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Pudenz-Schulte Medical Research Corp.. It received FDA 510(k) clearance on 1986-12-03 under 510(k) number K862907. 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 P-S MEDICAL CSF-SIPHON CONTROL DEVICE?

P-S MEDICAL CSF-SIPHON CONTROL DEVICE is a medical device that received FDA 510(k) clearance on 1986-12-03. The listed applicant is Pudenz-Schulte Medical Research Corp.. The 510(k) number is K862907.

When did P-S MEDICAL CSF-SIPHON CONTROL DEVICE receive FDA 510(k) clearance?

P-S MEDICAL CSF-SIPHON CONTROL DEVICE received FDA 510(k) clearance on 1986-12-03, under 510(k) number K862907.

Who is the listed applicant for P-S MEDICAL CSF-SIPHON CONTROL DEVICE?

The FDA 510(k) record lists Pudenz-Schulte Medical Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for P-S MEDICAL CSF-SIPHON CONTROL DEVICE?

The FDA product code for P-S MEDICAL CSF-SIPHON CONTROL DEVICE is JXG.

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Other records listing Pudenz-Schulte Medical Research Corp. 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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