The following data is part of a premarket notification filed by Porter Instrument Co., Inc. with the FDA for Mxr-2000 Flowmeter.
Device ID | K923781 |
510k Number | K923781 |
Device Name: | MXR-2000 FLOWMETER |
Classification | Flowmeter, Tube, Thorpe, Back-pressure Compensated |
Applicant | PORTER INSTRUMENT CO., INC. COLUMBIA SQUARE 555 THIRTEENTH ST., N.W. Washington, DC 20004 |
Contact | & Hartson |
Correspondent | & Hartson PORTER INSTRUMENT CO., INC. COLUMBIA SQUARE 555 THIRTEENTH ST., N.W. Washington, DC 20004 |
Product Code | CAX |
CFR Regulation Number | 868.2340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-07-28 |
Decision Date | 1993-06-10 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00816711020691 | K923781 | 000 |
00816711020059 | K923781 | 000 |
00816711020066 | K923781 | 000 |
00816711020073 | K923781 | 000 |
00816711020080 | K923781 | 000 |
00816711020325 | K923781 | 000 |
00816711020332 | K923781 | 000 |
00816711020349 | K923781 | 000 |
00816711020356 | K923781 | 000 |
00816711020646 | K923781 | 000 |
00816711020653 | K923781 | 000 |
00816711020011 | K923781 | 000 |