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FDA 510(k)

HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR.

K-Number: K871271 · 1987-09-15

ApplicantHuntleigh Technology, Inc.
Decision Date1987-09-15
Product CodeDRM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR. is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Technology, Inc.. It received FDA 510(k) clearance on 1987-09-15 under 510(k) number K871271. The device is classified under product code DRM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR.?

HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR. is a medical device that received FDA 510(k) clearance on 1987-09-15. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K871271.

When did HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR. receive FDA 510(k) clearance?

HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR. received FDA 510(k) clearance on 1987-09-15, under 510(k) number K871271.

Who is the listed applicant for HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR.?

The FDA 510(k) record lists Huntleigh Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR.?

The FDA product code for HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR. is DRM.

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Other records listing Huntleigh Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K992733AKRON ATP9 TRACTION MACHINEK964699RHEO DOPPLEX II (RD 2)K924516OP3/VP4K910188FLOWPLUS AC330 PUMP GARMENTSK900882MULTI DOPPLEX, MD-1K900618HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140

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Related Devices (Code: DRM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K221700AutoPulse NXT Resuscitation SystemZoll Circulation, Inc.K211289RMU-2000 Automated Chest Compression SystemDefibtech, LLCK173553LUCAS 3 Chest Compression SystemJolife ABK161768LUCAS 3 Chest Compression SystemJolife ABK153628ROSC-U Mini Chest Compressor (RMCC)Resuscitation International, LLCK112998AUTOPULSE RESUSCITATION SYSTEM MODEL 1000Zoll Circulation

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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