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FDA 510(k)

I.M PROBES

K-Number: K802951 · 1980-12-17

ApplicantHogan & Hartson
Decision Date1980-12-17
Product CodeHXB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

I.M PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1980-12-17 under 510(k) number K802951. The device is classified under product code HXB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.M PROBES?

I.M PROBES is a medical device that received FDA 510(k) clearance on 1980-12-17. The listed applicant is Hogan & Hartson. The 510(k) number is K802951.

When did I.M PROBES receive FDA 510(k) clearance?

I.M PROBES received FDA 510(k) clearance on 1980-12-17, under 510(k) number K802951.

Who is the listed applicant for I.M PROBES?

The FDA 510(k) record lists Hogan & Hartson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I.M PROBES?

The FDA product code for I.M PROBES is HXB.

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Other records listing Hogan & Hartson 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.

K974168COOPERSURGICAL INFRARED COAGULATORK973849BIOABSORBABLE BANKART TACKK973162DUAL RADIATION TARGETING SYSTEM DRTS DRAPEK950169RIBOSOMAL P EIA TEST SYSTEMK942389TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVESK946216CARDIOLIPIN A EIA TEST SYSTEM

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Related Devices (Code: HXB)

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.

K960539DIAO HAND SURGERY SETKinetikos Medical, Inc.K943472COHORT AVB RETRACTOR SYSTEMCohort Medical Products Group, Inc.K912843FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBEFlexmedicsK890227SURGICAL PROBEKinetic Medical ProductsK873651BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375Arthropedics, Inc.K873652HOOK PROBE #TM-1376Arthropedics, Inc.

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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