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FDA 510(k)

AERO PULSE ALTERNATING PRES. PUMP

K-Number: K771463 · 1977-08-26

ApplicantMedline Industries, Inc.
Decision Date1977-08-26
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AERO PULSE ALTERNATING PRES. PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1977-08-26 under 510(k) number K771463. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AERO PULSE ALTERNATING PRES. PUMP?

AERO PULSE ALTERNATING PRES. PUMP is a medical device that received FDA 510(k) clearance on 1977-08-26. The listed applicant is Medline Industries, Inc.. The 510(k) number is K771463.

When did AERO PULSE ALTERNATING PRES. PUMP receive FDA 510(k) clearance?

AERO PULSE ALTERNATING PRES. PUMP received FDA 510(k) clearance on 1977-08-26, under 510(k) number K771463.

Who is the listed applicant for AERO PULSE ALTERNATING PRES. PUMP?

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

What is the FDA product code for AERO PULSE ALTERNATING PRES. PUMP?

The FDA product code for AERO PULSE ALTERNATING PRES. PUMP is FNM.

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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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