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FDA 510(k)

SACCOMANNO SPECIMAN SOLUTION

K-Number: K862725 · 1986-08-01

ApplicantMill-Rose Laboratory
Decision Date1986-08-01
Product CodeLDZ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

SACCOMANNO SPECIMAN SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Mill-Rose Laboratory. It received FDA 510(k) clearance on 1986-08-01 under 510(k) number K862725. The device is classified under product code LDZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SACCOMANNO SPECIMAN SOLUTION?

SACCOMANNO SPECIMAN SOLUTION is a medical device that received FDA 510(k) clearance on 1986-08-01. The listed applicant is Mill-Rose Laboratory. The 510(k) number is K862725.

When did SACCOMANNO SPECIMAN SOLUTION receive FDA 510(k) clearance?

SACCOMANNO SPECIMAN SOLUTION received FDA 510(k) clearance on 1986-08-01, under 510(k) number K862725.

Who is the listed applicant for SACCOMANNO SPECIMAN SOLUTION?

The FDA 510(k) record lists Mill-Rose Laboratory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SACCOMANNO SPECIMAN SOLUTION?

The FDA product code for SACCOMANNO SPECIMAN SOLUTION is LDZ.

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Other records listing Mill-Rose Laboratory 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.

K983122MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) COMBINATION CYTOLOGY/HISTOLOGY PROCEDURAL KITK983124MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) CYTOLOGY PROCEDURAL KITK971275MILL-ROSE DISPOSABLE POLYPECTOMY SNAREK962736MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLEK960880MILL-ROSE BLIND MICROBIOLOGY BRUSHK954519WANG TRANSENDOSCOPIC ASPIRATION NEEDLE

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Related Devices (Code: LDZ)

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.

K883048ATS PARA-SET MODIFIED PVA FIXATIVE SOLUTIONAlpha-Tec Systems, Inc.K881922CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVESurgipath Medical Industries, Inc.K881698ATS PVA FIXATIVE SOLUTIONAlpha-Tec Systems, Inc.K843428BIOFIXAccra Laboratories, Inc.K842913WRIGHT STAIN FIXATIVEE K Ind., Inc.K831061PVA FIXATIVE/FORMALINAmerican Micro Scan

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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