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FDA 510(k)

SPATULA FOR PAP SMEAR COLLECTION

K-Number: K893229 · 1990-02-22

ApplicantMedical Device Inspection Co., Inc.
Decision Date1990-02-22
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SPATULA FOR PAP SMEAR COLLECTION is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Inspection Co., Inc.. It received FDA 510(k) clearance on 1990-02-22 under 510(k) number K893229. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPATULA FOR PAP SMEAR COLLECTION?

SPATULA FOR PAP SMEAR COLLECTION is a medical device that received FDA 510(k) clearance on 1990-02-22. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K893229.

When did SPATULA FOR PAP SMEAR COLLECTION receive FDA 510(k) clearance?

SPATULA FOR PAP SMEAR COLLECTION received FDA 510(k) clearance on 1990-02-22, under 510(k) number K893229.

Who is the listed applicant for SPATULA FOR PAP SMEAR COLLECTION?

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

What is the FDA product code for SPATULA FOR PAP SMEAR COLLECTION?

The FDA product code for SPATULA FOR PAP SMEAR COLLECTION is HHT.

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Other records listing Medical Device Inspection Co., Inc. as applicant

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Related Devices (Code: HHT)

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.

K182049exCellerator Cervical Collection DeviceExcell Company, LLCK153128Kolplast Cervical Sample Collection KitKolplast CI SAK111681HISTOBRUSHPuritan Medical Products Company, LLCK083012PAPCONEOtto Bock Pur Life Science GmbHK081522BIO NUCLEAR DIAGNOSTICS (ENDO)CERVICAL SAMPLER FOR GYN CYTOLOGYBio Nuclear Diagnostics, Inc.K072381SOFTPAP CERVICAL CELL COLLECTORCytocore, 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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