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FDA 510(k)

IMPACT MODELS 701, 702 AND 703

K-Number: K861272 · 1986-05-20

ApplicantImpact Instrumentation, Inc.
Decision Date1986-05-20
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

IMPACT MODELS 701, 702 AND 703 is the device name listed in this FDA 510(k) record. The listed applicant is Impact Instrumentation, Inc.. It received FDA 510(k) clearance on 1986-05-20 under 510(k) number K861272. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPACT MODELS 701, 702 AND 703?

IMPACT MODELS 701, 702 AND 703 is a medical device that received FDA 510(k) clearance on 1986-05-20. The listed applicant is Impact Instrumentation, Inc.. The 510(k) number is K861272.

When did IMPACT MODELS 701, 702 AND 703 receive FDA 510(k) clearance?

IMPACT MODELS 701, 702 AND 703 received FDA 510(k) clearance on 1986-05-20, under 510(k) number K861272.

Who is the listed applicant for IMPACT MODELS 701, 702 AND 703?

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

What is the FDA product code for IMPACT MODELS 701, 702 AND 703?

The FDA product code for IMPACT MODELS 701, 702 AND 703 is BTL.

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Other records listing Impact Instrumentation, Inc. as applicant

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Related Devices (Code: BTL)

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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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