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FDA 510(k)

PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN

K-Number: K853497 · 1985-08-28

Decision Date1985-08-28
Product CodeIFP
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN is the device name listed in this FDA 510(k) record. The listed applicant is Surgipath Medical Industries, Inc.. It received FDA 510(k) clearance on 1985-08-28 under 510(k) number K853497. 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 PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN?

PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN is a medical device that received FDA 510(k) clearance on 1985-08-28. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K853497.

When did PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN receive FDA 510(k) clearance?

PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN received FDA 510(k) clearance on 1985-08-28, under 510(k) number K853497.

Who is the listed applicant for PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN?

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

What is the FDA product code for PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN?

The FDA product code for PREFILLED SPECIMEN JARS 10% NEUTRAL BUF-FORMALIN 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.

Other records listing Surgipath Medical Industries, 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.

View all 30 devices →

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.

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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