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FDA 510(k)

PARAMETRIC PROCESS CONTROL

K-Number: K923826 · 1992-10-22

ApplicantScimed Life Systems, Inc.
Decision Date1992-10-22
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PARAMETRIC PROCESS CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Scimed Life Systems, Inc.. It received FDA 510(k) clearance on 1992-10-22 under 510(k) number K923826. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAMETRIC PROCESS CONTROL?

PARAMETRIC PROCESS CONTROL is a medical device that received FDA 510(k) clearance on 1992-10-22. The listed applicant is Scimed Life Systems, Inc.. The 510(k) number is K923826.

When did PARAMETRIC PROCESS CONTROL receive FDA 510(k) clearance?

PARAMETRIC PROCESS CONTROL received FDA 510(k) clearance on 1992-10-22, under 510(k) number K923826.

Who is the listed applicant for PARAMETRIC PROCESS CONTROL?

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

What is the FDA product code for PARAMETRIC PROCESS CONTROL?

The FDA product code for PARAMETRIC PROCESS CONTROL is LIT.

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Other records listing Scimed Life Systems, 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.

K974241SCIMED INFORMER PRESSURE WIRE SYSTEMK981788SCIMED 6 FRENCH WISEGUIDE GUIDE CATHETERK980360SCIMED QUEST FLOPPY AND MODERATE SUPPORT GUIDE WIRESK974559SCIMED 6 FRENCH IMPULSE ANGIOGRAPHIC CATHETERSK974684SCIMED 7 FRENCH WISEGUIDE GUIDE CATHETERK973945LUGE GUIDE WIRE

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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