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FDA 510(k)

SALT CREEK P.I. TRAY

K-Number: K864682 · 1987-01-06

ApplicantSalt Creek Medical Technologies
Decision Date1987-01-06
Product Code
DecisionSubstantially Equivalent

Device Summary

SALT CREEK P.I. TRAY 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 1987-01-06 under 510(k) number K864682. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALT CREEK P.I. TRAY?

SALT CREEK P.I. TRAY is a medical device that received FDA 510(k) clearance on 1987-01-06. The listed applicant is Salt Creek Medical Technologies. The 510(k) number is K864682.

When did SALT CREEK P.I. TRAY receive FDA 510(k) clearance?

SALT CREEK P.I. TRAY received FDA 510(k) clearance on 1987-01-06, under 510(k) number K864682.

Who is the listed applicant for SALT CREEK P.I. TRAY?

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

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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, 250CCK871087S.C.M.T. PERFORATORK871075SCMT UMBILICAL CLAMPK864296S.C.T. MULTI PORT, INJECTION SITEK864692EXTENSION SETS

View all 8 devices →

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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