510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K843593Substantially Equivalent

Surgipress Surgical Loop

Syntex Corp., Palo Alto CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K843593 is the FDA 510(k) clearance record for SURGIPRESS SURGICAL LOOP, a class I device, cleared for Syntex Corp. on under FDA product code HRQ (Hemostat). FDA records list 10 510(k) clearances for Syntex Corp., from to . As of , FDA records show no recalls naming K843593.

Clearance record

Decision date
Received
(42 days to decision)
Product code
HRQ Hemostat
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Syntex Corp. 3401 Hillview Ave., Palo Alto CA
Third party review
No

Clearances, product code HRQ

Trailing 12 months

FDA records hold no clearances under product code HRQ in the trailing twelve months.

FDA records show no clearances under product code HRQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HRQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260