FDA 510(k)

VAC-RITE

K-Number: K770649 · 1977-06-02

Decision Date1977-06-02

Product CodeKDQ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VAC-RITE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Development Co.. It received FDA 510(k) clearance on 1977-06-02 under 510(k) number K770649. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAC-RITE?

VAC-RITE is a medical device that received FDA 510(k) clearance on 1977-06-02. The listed applicant is Medical Development Co.. The 510(k) number is K770649.

When did VAC-RITE receive FDA 510(k) clearance?

VAC-RITE received FDA 510(k) clearance on 1977-06-02, under 510(k) number K770649.

Who is the listed applicant for VAC-RITE?

The FDA 510(k) record lists Medical Development Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAC-RITE?

The FDA product code for VAC-RITE is KDQ.

Other records listing Medical Development Co. 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.

K770758INJECTION SYSTEM, MDC I.V.

Related Devices (Code: KDQ)

K081718EXPRESS CHEST DRAINAtrium Medical Corp.K062302MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEMMillicore AB K043582OCEAN CHEST DRAINAtrium Medical Corp.K984496ATRIUM MEDICAL CORPORATION EXPRESS CHEST DRAINAtrium Medical Corp.K962856PLEUR-EVAC SAHARA ADULT/PEDIATRIC CHEST DRAINAGE SYSTEM MODEL S-1100, S-1200, 2-2100, AND S-2200 WITH MODEL S-100 AUTOTRDeknatel, Inc.K961287ROCKET PLEURASEAL II CHEST DRAINAGE SYSTEMRocket Medical Plc

Official Source

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