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FDA 510(k)

TECA MODEL SP5/T ELECTRO-THER. STIM.

K-Number: K761220 · 1976-12-17

ApplicantTeca, Inc.
Decision Date1976-12-17
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TECA MODEL SP5/T ELECTRO-THER. STIM. is the device name listed in this FDA 510(k) record. The listed applicant is Teca, Inc.. It received FDA 510(k) clearance on 1976-12-17 under 510(k) number K761220. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECA MODEL SP5/T ELECTRO-THER. STIM.?

TECA MODEL SP5/T ELECTRO-THER. STIM. is a medical device that received FDA 510(k) clearance on 1976-12-17. The listed applicant is Teca, Inc.. The 510(k) number is K761220.

When did TECA MODEL SP5/T ELECTRO-THER. STIM. receive FDA 510(k) clearance?

TECA MODEL SP5/T ELECTRO-THER. STIM. received FDA 510(k) clearance on 1976-12-17, under 510(k) number K761220.

Who is the listed applicant for TECA MODEL SP5/T ELECTRO-THER. STIM.?

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

What is the FDA product code for TECA MODEL SP5/T ELECTRO-THER. STIM.?

The FDA product code for TECA MODEL SP5/T ELECTRO-THER. STIM. is IPF.

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Other records listing Teca, Inc. as applicant

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Related Devices (Code: IPF)

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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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