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FDA 510(k)

JACOBS HIGH VACUUM SUCTION UNIT 05-2570

K-Number: K843693 · 1984-10-31

ApplicantJ. Sklar Mfg. Co., Inc.
Decision Date1984-10-31
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

JACOBS HIGH VACUUM SUCTION UNIT 05-2570 is the device name listed in this FDA 510(k) record. The listed applicant is J. Sklar Mfg. Co., Inc.. It received FDA 510(k) clearance on 1984-10-31 under 510(k) number K843693. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JACOBS HIGH VACUUM SUCTION UNIT 05-2570?

JACOBS HIGH VACUUM SUCTION UNIT 05-2570 is a medical device that received FDA 510(k) clearance on 1984-10-31. The listed applicant is J. Sklar Mfg. Co., Inc.. The 510(k) number is K843693.

When did JACOBS HIGH VACUUM SUCTION UNIT 05-2570 receive FDA 510(k) clearance?

JACOBS HIGH VACUUM SUCTION UNIT 05-2570 received FDA 510(k) clearance on 1984-10-31, under 510(k) number K843693.

Who is the listed applicant for JACOBS HIGH VACUUM SUCTION UNIT 05-2570?

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

What is the FDA product code for JACOBS HIGH VACUUM SUCTION UNIT 05-2570?

The FDA product code for JACOBS HIGH VACUUM SUCTION UNIT 05-2570 is BTA.

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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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