Cleared Traditional

K771199 - SURGIPULSE HEART RATE MONITOR

K771199 is the FDA 510(k) clearance for SURGIPULSE HEART RATE MONITOR by Stryker Corp.. It is a Class 2 Cardiovascular device (product code DRT) cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K771199 · Stryker Corp. · Cardiovascular device
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Jul 1977
Decision
20d
Days
Class 2
Risk

K771199 is an FDA 510(k) clearance for the SURGIPULSE HEART RATE MONITOR. Classified as Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm) (product code DRT), Class II - Special Controls.

Submitted by Stryker Corp. (Mchenry, US). The FDA issued a Cleared decision on July 25, 1977 after a review of 20 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2300 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Stryker Corp. devices

Submission Details

510(k) Number K771199 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 05, 1977
Decision Date July 25, 1977
Days to Decision 20 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
105d faster than avg
Panel avg: 125d · This submission: 20d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DRT Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2300
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - DRT Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm)

All 148
Devices cleared under the same product code (DRT) and FDA review panel - the closest regulatory comparables to K771199.
HEARTRATE METER MODEL 650, P/N 000119
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K770022 · Hewlett-Packard Co. · Feb 1977
MONITOR, NEONATE, MODEL 78213A
K770023 · Hewlett-Packard Co. · Feb 1977
MONITOR, NEONATAL, MODEL 78260A
K770024 · Hewlett-Packard Co. · Feb 1977