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FDA 510(k)

PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS

K-Number: K851464 · 1985-07-05

ApplicantPulse Med, Inc.
Decision Date1985-07-05
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS is the device name listed in this FDA 510(k) record. The listed applicant is Pulse Med, Inc.. It received FDA 510(k) clearance on 1985-07-05 under 510(k) number K851464. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS?

PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS is a medical device that received FDA 510(k) clearance on 1985-07-05. The listed applicant is Pulse Med, Inc.. The 510(k) number is K851464.

When did PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS receive FDA 510(k) clearance?

PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS received FDA 510(k) clearance on 1985-07-05, under 510(k) number K851464.

Who is the listed applicant for PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS?

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

What is the FDA product code for PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS?

The FDA product code for PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS is FMF.

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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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