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FDA 510(k)

CONPHAR FINGERTIP SUCTION CONTROL

K-Number: K791801 · 1979-09-21

ApplicantConphar, Inc.
Decision Date1979-09-21
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONPHAR FINGERTIP SUCTION CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1979-09-21 under 510(k) number K791801. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR FINGERTIP SUCTION CONTROL?

CONPHAR FINGERTIP SUCTION CONTROL is a medical device that received FDA 510(k) clearance on 1979-09-21. The listed applicant is Conphar, Inc.. The 510(k) number is K791801.

When did CONPHAR FINGERTIP SUCTION CONTROL receive FDA 510(k) clearance?

CONPHAR FINGERTIP SUCTION CONTROL received FDA 510(k) clearance on 1979-09-21, under 510(k) number K791801.

Who is the listed applicant for CONPHAR FINGERTIP SUCTION CONTROL?

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

What is the FDA product code for CONPHAR FINGERTIP SUCTION CONTROL?

The FDA product code for CONPHAR FINGERTIP SUCTION CONTROL is JOL.

Related Clinical Trials

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.

Other records listing Conphar, 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.

View all 122 devices →

Related Devices (Code: JOL)

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.

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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