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FDA 510(k)

S.C.M.T. PERFORATOR

K-Number: K871087 · 1987-03-23

ApplicantSalt Creek Medical Technologies
Decision Date1987-03-23
Product CodeHGE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

S.C.M.T. PERFORATOR is the device name listed in this FDA 510(k) record. The listed applicant is Salt Creek Medical Technologies. It received FDA 510(k) clearance on 1987-03-23 under 510(k) number K871087. The device is classified under product code HGE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S.C.M.T. PERFORATOR?

S.C.M.T. PERFORATOR is a medical device that received FDA 510(k) clearance on 1987-03-23. The listed applicant is Salt Creek Medical Technologies. The 510(k) number is K871087.

When did S.C.M.T. PERFORATOR receive FDA 510(k) clearance?

S.C.M.T. PERFORATOR received FDA 510(k) clearance on 1987-03-23, under 510(k) number K871087.

Who is the listed applicant for S.C.M.T. PERFORATOR?

The FDA 510(k) record lists Salt Creek Medical Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for S.C.M.T. PERFORATOR?

The FDA product code for S.C.M.T. PERFORATOR is HGE.

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Other records listing Salt Creek Medical Technologies 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.

K864683NEONATAL FEEDING KITK871042URINE METER, 250CCK871075SCMT UMBILICAL CLAMPK864296S.C.T. MULTI PORT, INJECTION SITEK864682SALT CREEK P.I. TRAYK864692EXTENSION SETS

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Related Devices (Code: HGE)

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.

K951148OBSTI-HOOKOnliK926425AMNIPERF(TM)Raymart Development Co.K910518GLOVE-N-GEL AMNIOTOMY KITEpcom Medical Systems, Inc.K850758AMNIGLOVE & AMNICOTGo Medical Industries Pty. , Ltd.K834177H.R. JAKOBI SURG. INSTRUMENTS #4 30/31Imm Enterprises , 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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