FDA 510(k)

PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR

K-Number: K915170 · 1992-07-28

Decision Date1992-07-28

Product CodeMED

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Pymah Corp.. It received FDA 510(k) clearance on 1992-07-28 under 510(k) number K915170. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR?

PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR is a medical device that received FDA 510(k) clearance on 1992-07-28. The listed applicant is Pymah Corp.. The 510(k) number is K915170.

When did PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR receive FDA 510(k) clearance?

PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR received FDA 510(k) clearance on 1992-07-28, under 510(k) number K915170.

Who is the listed applicant for PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR?

The FDA 510(k) record lists Pymah Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR?

The FDA product code for PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR is MED.

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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.