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FDA 510(k)

DISTOMETER

K-Number: K882575 · 1988-07-01

ApplicantHagg-Streit Service, Inc.
Decision Date1988-07-01
Product CodeHMM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DISTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Hagg-Streit Service, Inc.. It received FDA 510(k) clearance on 1988-07-01 under 510(k) number K882575. The device is classified under product code HMM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISTOMETER?

DISTOMETER is a medical device that received FDA 510(k) clearance on 1988-07-01. The listed applicant is Hagg-Streit Service, Inc.. The 510(k) number is K882575.

When did DISTOMETER receive FDA 510(k) clearance?

DISTOMETER received FDA 510(k) clearance on 1988-07-01, under 510(k) number K882575.

Who is the listed applicant for DISTOMETER?

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

What is the FDA product code for DISTOMETER?

The FDA product code for DISTOMETER is HMM.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Hagg-Streit Service, 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.

K800238MOIRE FRINGE VISOMETER AFTER LOTMAR

Related Devices (Code: HMM)

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.

K873440RULE, PUPILLARYAllegheny Plastics, 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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