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FDA 510(k)

AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000

K-Number: K981754 · 1998-06-16

ApplicantPorter Instrument Co., Inc.
Decision Date1998-06-16
Product CodeCBN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000 is the device name listed in this FDA 510(k) record. The listed applicant is Porter Instrument Co., Inc.. It received FDA 510(k) clearance on 1998-06-16 under 510(k) number K981754. The device is classified under product code CBN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000?

AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000 is a medical device that received FDA 510(k) clearance on 1998-06-16. The listed applicant is Porter Instrument Co., Inc.. The 510(k) number is K981754.

When did AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000 receive FDA 510(k) clearance?

AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000 received FDA 510(k) clearance on 1998-06-16, under 510(k) number K981754.

Who is the listed applicant for AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000?

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

What is the FDA product code for AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000?

The FDA product code for AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000 is CBN.

Related Clinical Trials

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Other records listing Porter Instrument Co., 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.

K062155DIGITAL MXR-D FLOWMETERK924596SES-2012 AUTOMATIC STEAM STERILIZERK923781MXR-2000 FLOWMETERK895638STEAM STERILIZER (AUTOCLAVE), DENTALK802067CLEAN-AIR POLLUTION REDUCTION SYSTEM

Related Devices (Code: CBN)

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.

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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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