510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K913997Substantially Equivalent

Saecg Cardiograph Model M1754a

Hewlett-Packard Co., Mcminnville OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913997 is the FDA 510(k) clearance record for SAECG CARDIOGRAPH MODEL M1754A, a class II device, cleared for Hewlett-Packard Co. on under FDA product code KNT (Tubes, Gastrointestinal (And Accessories)). FDA records list 246 510(k) clearances for Hewlett-Packard Co., from to . As of , FDA records show no recalls naming K913997.

Clearance record

Decision date
Received
(182 days to decision)
Product code
KNT Tubes, Gastrointestinal (And Accessories)
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Hewlett-Packard Co. 1700 S. Baker St., Mcminnville OR
510(k) summary
Statement
Third party review
No

Clearances, product code KNT

Trailing 12 months
3 clearances under product code KNT in the twelve months to November 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KNT, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20261
September 20261
October 20260
November 20260