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FDA 510(k)

(MSI) PATH-SAVER

K-Number: K872140 · 1987-06-15

ApplicantMedical Specialties, Inc.
Decision Date1987-06-15
Product CodeIFP
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

(MSI) PATH-SAVER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Specialties, Inc.. It received FDA 510(k) clearance on 1987-06-15 under 510(k) number K872140. The device is classified under product code IFP. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the (MSI) PATH-SAVER?

(MSI) PATH-SAVER is a medical device that received FDA 510(k) clearance on 1987-06-15. The listed applicant is Medical Specialties, Inc.. The 510(k) number is K872140.

When did (MSI) PATH-SAVER receive FDA 510(k) clearance?

(MSI) PATH-SAVER received FDA 510(k) clearance on 1987-06-15, under 510(k) number K872140.

Who is the listed applicant for (MSI) PATH-SAVER?

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

What is the FDA product code for (MSI) PATH-SAVER?

The FDA product code for (MSI) PATH-SAVER is IFP.

Related Clinical Trials

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.

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Other records listing Medical Specialties, 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.

K946201STAND, INFUSIONK931947CHECKPOINTK926095REFRACTROL-SPK924926MSI-HCTK896566MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVEK883851MSI-CAL 8

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Related Devices (Code: IFP)

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.

K884755CONSED FECAL CONCENTRATION SYSTEMDonald L. Price, Ph.D.K872663DRY-FORMAnatech, Ltd.K870852NBF 10% NEUTRAL BUFFERED FORMALINAnatech, Ltd.K853497PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALINSurgipath Medical Industries, Inc.K842982FORMALIN BUFFEREDReagent Laboratory, Inc.K842940CBA FORMALINAnatech, 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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